CA1330567C - Tetralin esters of phenols or benzoic acids having retinoid like activity - Google Patents

Abstract

ABSTRACT

Retinoid-like activity is exhibited by compounds of the for-mula where the R groups are independently hydrogen, or lower alkyl; A
is -C(O)O-, -OC(O)-, -C(O)S-, or -SC(O)-; n is 0-5; and Z is H, -COB
where B is -OH or a pharmaceutically acceptable salt, or B is -OR1 where R1 is an ester-forming group, or B is -N(R)2 where R is hydrogen or lower alkyl, or Z is -OE where E is hydrogen or an ether-forming group or -COR2 where R2 is hydrogen, lower alkyl, phenyl or lower alkyl phenyl, or Z is -CHO or an acetal derivative thereof, or Z is -COR3 where R3 is -(CH2)mCH3 where m is 0-4 and the sum of n and m does not exceed 4.

Description

~33~67 ~ ~

Tetralin Esters of Phenols or ~enzoic Acids 2 ~ in~_;Retinoid Like Activity 3 :~ ~ ~

4 Ba~ck~round This invention relates to novel compounds having 6 retinoid-like activity. More specifically, the invention relates to 7 compounds comprising a tetralin ester of phenolic acids and ~ terephthallic acids. The acid function of the phenyl containing 9 moiety may also be converted to an alcohol, aldehyde or ketone or derivatives thereof, or that group may be alkyl or H.
.
12 BeJa~ Art 3 Compounds of similar nature wherein A is -C(O)-N(H)- are 4 discussed in an article in the Am. Academv of Dermatology. Sporn, 15 M.B., et al., V. 15, No. 4, p 756 (1986); a communication by 16 Kagechika, H., et al, in Chem. Pharm. Bull., 32, (10) 4209 (1984) 7 and another communication by Shudo, K, et al., in Chçm, Pbarm.
Bull., 33 (1) 404-407 (1985).
,~
S u m~ ~ /~ n~
iD This invention covers compounds of formula I

D ~(CH2)n-Z

u where the R groups are independently hydrogen, or lower alkyl; A
~ is -C(O)O-, -OC(O)-, -C(O)S-, or -SC(O)-; n is 0-5; and Z is H, -COB
27 where B is -OH or a pharmaceutically acceptable salt, or B is -OR

~-'' ~ ... . ... ...

~ 3 ~

~ where R1 is an ester-forming group, or B is ^N(R)2 where R is 2 hydrogen or lower alkyl, or Z is -OE where E is hydrogen or an 3 ether-forming group or-COR2 where R2 is hydrogen, lower alkyl, 4 phenyl or lower alkyl phenyl, or Z is -CHO or an acetal derivative 5 thereof, or Z is -COR3 where R3 is -(CH2)mCH3 where m is 0-4 and 6 the sum of n and m does not exceed 4.

7 In a second aspect, this invention relates to the use of the 8 compounds of formula I for treating dermatoses such as acne, 9 Darier's disease, psoriasis, icthyosis, eczema, atopic dermatitis and ~o epithelial cancers. These compounds are also useful in the '1 treatment of arthritic diseases and other immunological disorders 12 (e.g., lupus erythematosus), in promoting wound healing and in ~3 treating dry eye syndrome and in treating or reversing the effects ~4 of sun induced skin aging and damage.
~5 This invention also relates to a pharmaceutical formulation ~6 comprising a compound of formula I in admixture with a ~7 pharmaceutically acceptable excipient, particularly a composition having anti-psoriatic activity.
In another aspect, this invention relates to the process for making a compound of formula I which process comprises reacting 2, a compound where the X or Y of formula II or III is an acid or acid 72 derivative which can form an ester with the corresponding a formula II or III where X or Y is an -OH or -SH group, preferably ~4 in the presence of an ester-forming catalyst.

" R~XR ~(CH2~n-Z

Il 111 ; ~

133~7 where R, n and Z are the same as defined above.
2 To synthesize compounds where n is 1 or greater and th 3 corresponding formula III form is not commercially available, the acid of formula III where Z is COOH can be homologated to insert S the desired number of methylene groups. This homologation 6 product, the acid, ca~ then be reduced to give the corresponding 7 aldehyde or alcohol. Such compound can then be coupled with the ~ corresponding formula II compound, the Z functional group being g protected as necessary. Acids of formula I may be converted to lD their salts by treating them with the appropriate base under mild ~l conditions. An acid of formula I can also be converted to an ester.

l~ General ~mbodiments 1~ DefinitiQn~
16 The term "ester" as used here refers to and covers any 17 compound falling within the definition of that term as classically used in organic chemistry. Where Z is -COOH, this term covers the 19 products derived from treatment of this function with alcohols.
20 Examples are the Cl to C6 alkyl esters (lower alkyl) or Cl to C'6 lower alkyl phenyl esters. Where the ester is derived from compounds where Z is -OH, this term covers compounds of the formula OC(O)R' where R' is any substituted or unsubstituted aliphatic, aromatic or aliphatic-aromatic group, particularly those ~5 of 7 to 10 carbons.
26 Preferred esters are derived from the saturated aliphatic 2~ alcohols or acids of ten or fewer carbon atoms or the cyclic or ~ saturated aliphatic cyclic alcohols and acids of S to 10 carbon 29 atoms. Particularly preferred aliphatic esters are those derived 30 from lower alkyl acids and alcohols. Here, and where ever else ~? !~
l ~ " ~

~ r~, , .

~ 3 ~

~ used, lower alkyl means having 1-6 carbon atoms. Also preferred 2 are the phenyl or lower alkylphenyl esters.
3 Amide has the meaning classically accorded that term in 4 organic chemistry. In this instance it includes the unsubstituted 5 amides and all aliphatic and aromatic mono- and di-substituted 6 amides. Preferred amides are the mono- and di-substituted 7 amides derived from the saturated aliphatic radicals of ten or fewer carbon atoms or the cyclic or saturated aliphatic-cyclic g radicals of 5 to 10 carbon atoms. Particularly preferred amides are those derived from lower alkyl amines. Also preferred are mono- and di-substituted amides derived from the phenyl or ~2 lower alkylphenyl amines. Unsubstituted amides are also 13 preferred-l~ Acetals and ketals includes the radicals of the formula -CK
15 where K is (-OR')2. Here, R' is lower alkyl. Also, K may be -OR10-16 where Rl is lower alkyl of 2-5 carbon atoms, straight chain or 17 branched.
- A pharmaceutically acceptable salt may be prepared for any 17 compound of this invention having a functionality capable of forming such salt, for example an acid or an amine functionality.
A pharmaceutically acceptable salt may be any salt which retains the activity of the parent compound and does not impart any -deleterious or untoward effect on the subject to which it is administered in the context in which it is administered. ~ ~ -Such a salt may be derived from any organic or inorganic acid -2C or base. The salt may be a mono or polyvalent ion. Of particular 77 interest where the acid function is concerned are the inorganic ~ ions, sodium, potassium, calcium, and magnesium. Organic amine 29 salts may be made with amines, particularly ammonium salts such 30 as mono-, di- and trialkyl amines or ethanol amines. Salts may ~33~7 ~ also be formed with caffeine, tromethamine and similar molecules.
2 Where there is a nitrogen sufficeintly basic as to be capable of 3 forming acid addition salts, such may be forrned with any 4 inorganic or organic acids or alkylating agent such a methyl iodide.
Preferred acid addition salts are those formed with inorganic acids 6 such as hydrochloric acid, sulfuric acid or phosphoric acid. Any of 7 a number of simple organic acids having one, two or three ' carboxyl groups may be used for making acid addition salts. I
g Herein, the following numbering system is used for the instant compounds.

12 7 ~A~¢~

14 The preferred compounds of this invention are:
15 ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-16 2-naphthoyloxy)benzoate 17 benzyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-- 2-naphthoyloxy)benzoate, 19 pentadeuteroethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-20 tetrahydro-2-naphthoyloxy)benzoate, 21 n-hexyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-22 2-naphthoyloxy)benzoate, a n-tetradecyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetra-24 hydro-2-naphthoyloxy)benzoate, ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-26 2-naphthoyloxy)-3-methylbenzoate, 27 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-~ naphthoyloxy)benzamide, " .

1 663g , , ,., . . - .. : - ,. ~ . ~- , . , ~` ~ ~
~33~7 , .
4-methoxymethyl)phenyl)-5,~,8,8-tetramethyl-5,6,7,8-tetrah-2 ydro-2-naphthoate, 3 4-tert-butyldimethylsiloxymethy)lphenyl)-5,5,8,8-4 tetramethyl-5,6,7,8-tetrahydro-2-naphthoate, 4-formylphenyl)-5,5,8,8-tetramethyl-5,6,7,8-6 tetrahydro-2-naphthoate, 7 4-dimethoxymethylphenyl)-5,5,8,8-tetramethyl-5,6,7,8-' tetrahydro-2-naphthoate, 9 ethyl 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate, ll benzyl 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-12 naphthoyloxy)benzoate, 13 4-methoxymethylphenyl-3,5,5,8,8-pentamethyl-14 5,6,7,8-tetrahydro-2-naphthoate, '~ 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-16 naphthoyloxy)benzoic acid, 17 ethyl 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyl-18 oxy)benzoate, 19 benzyl 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyl- ~ ~ :
x oxy)benzoate~
2, 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)- :
Z benzoic acid, benzyl (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2- ; :~
naphthyl)terephthalate, ethyl (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-~ naphthyl)terephthalate, and ~ (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)-~ hydrogenterephthalate.
~ The compounds of this invention may be administered sys-temically or topically, depending on such considerations as the J
i ., .

.
~,"~ ~ ',,`'"~,, ~ ,,~ ' ,' ',, ," ' '` ' ' 133~67 l condition to be treated, need for site-specific treatment, quantity 2 of drug to be administered, and similar considerations.
3 In the treatment of dermatoses, it will generally be preferred 4 to administer the drug topically, though in certain cases such as 5 treatment of severe cystic acne, oral administration may also be 6 useful.
7 Any common topical formulation such as a solution, ' suspension, gel, ointment, or salve and the like may be used.
5 Preparation of such topical formulations are well described in the art of pharmaceutical formulations as exemplified, for example, in ll Remin~ton's Pharmaceutical Science. Edition 17, Mack Publishing 12 Company, Easton, Pennsylvania. For topical application, these 3 compounds could also be administered as a powder or spray, particularly in aerosol form.
~' Other medicaments can be added to such topical formulation 16 for such secondary purposes as treating skin dryness, providing ~7 protection against light; other medications for treating dermatoses, preventing infection, reducing irritation, inflammation and the 9 like.
If the drug is to be administered systemically, it may be 21 confected as a powder, pill, tablet or the like, or as a syrup or elixir for oral administration. For intravenous or intraperitoneal administration, the compound will be prepared as a solution or " suspension capable of being administered by injection. In certain cases, it may be useful to formulate these compounds in suppository form or as an extended release formulation for ~7 deposit under the skin or for intramuscular injection.
Treatment of dermatoses or any other indications known or 29 discovered to be susceptible to treatment by retinoic acid-like 30 compounds will be effected by administration of the ,, .

, 16639 .

~' ~
i ~:~ . . .. . .

1 33 ~f i~f ~ i~

~ therapeutically effective dose of one or more compounds of the 2 instant invention. A therapeutic concentration will be that 3 concentration which effects reduction of the particular condition, ~ or retards its expansion. In certain instances, the drug potentially 5 could be used in a prophylactic manner to prevent onset of a 6 particular condition. A given therapeutic concentration will vary 7 from condition to condition and in certain instances may vary with -the severity of the condition being treated and the patient's 5 susceptibility to treatment. Accordingly, a given therapeutic concentration will be best determined at the time and place lJ through routine experimentation. However, it is anticipated that in the treatment of, for example, acne, or other such dermatoses, 3 that a topical formulation containing between 0.01 and 0.5 milligrams per milliliter of formulation will constitute a ~ therapeutically effective concentration. If administered 16 systemically, an amount between 0.01 and 2 mg per kg body weight per day will effect a therapeutic or prophylatic result in most instances.
19 The retinoic acid-like activity of these compounds was D confirmed through the classic measure of retinoic acid activity ~i involving the effect of retinoic acid on ornithine decarboxylase.
Z The original work on the correlation between retinoic acid and ~ decrease in cell proliferation was done by Verma & Boutwell, -.
. Cancer Research. 1977. 37. 2196-2201. That reference discloses ~ that ornithine decarboxylase (ODC) activity increased precedent to 26 polyamine biosynthesis. It has been established elsewhere that increases in polyamine synthesis can be correlated or associated ~i with cellular proliferation. Thus, if ODC activity could be inhibited, cell hyperproliferation could be modulaled. Although all causes 30 for ODC activity increase are unknown, it is known that ~, .

. I . .

. ,~ .
,; .
, ;. ~ ~ . ~ ~. . . , . . , ~ . , ,,~3;` ~

~ 330~

l 12-0-tetradecanoylphorbol-13-acetate (TPA) induces ODC activity.
2 Retinoic acid inhibits this induction of ODC activity by TPA. The 3 compounds of this invention also inhibit TPA induction of ODC as demonstrated by an assay essentially following the procedure set out in Cancer Re~.: 1662-1670, 1975.

Specific Embodiments The compound of this invention can be made by a number of 9 different synthetic chemical pathways. To illustrate this invention, there is here outlined a series of steps which have been ll proven to provide the compounds of formula I when such 12 synthesis is followed in fact and in spirit. The synthetic chemist 13 will readily appreciate that the conditions set out here are specific embodiments which can be generalized to any and all of the ~' compounds represented by formula I.
16 Compounds of formula I where A is -C(O)O- are prepared as 17 follows:
,. .
19 Reaction Scheme I i -~OH HCl ~XC1 ~ ~
OH l><Cl ~COOH

',' ' "
-~3~7 --( CH2)n ~Z ~ ~, R ~1 ~(CH2)n~Z

3 The case where position 2 on the tetrahydronaphthalene ring is 4 alkyl (methyl) are made as follows, Scheme IA.

~H HQ

\

HO~ ~OH _ ~

This reaction flow diagram illustrates specific compounds, but : 9 these illustrations can be generalized to all compounds disclosed herein including those where A is C(O)S or SC(O), by varying the ~ starting mateTials or selecting the appropriate intermediate.
2 Compounds of formula I where A is -C(O)O-, and only the 5 or 3 8 positions on the tetrahydronaphthalene are methyl (alkyl) are 4 prepared as per Reaction Scheme II.
Reaction Scheme II

1. ~Ig/Ether kOH
Br `~6~
2. d~methyl 9 ~ I -ketone 1 lB1 lA 10 1 2 13 ~ ~(CHz)n~Z

9 ' l~o~

Compounds of formula I where A is -OC(O)- are prepared as per Reaction Scheme III.

l6639 ~ 3 ~

Reaction Scheme III
2 :
R R ~:
R~,R + ~OH AlCl3 ~OH

5~CoOH C~)COOR ~)COOR

[~ ~(CH2)n-~
R R

A general description for making the compounds recited in 6 the foregoing schemes follows.
7 The 2,5-dihydroxy-2,5-dimethylhexane of formula 1 is ~ converted to its corresponding dichloride of formula 2 by treating 9 the dihydroxy compound with hydrogen chloride gas. The o reaction is effected at room temperature or thereabout by ll bubbling hydrogen chloride gas through an aqueous hydrochloric 12 acid suspension of the dihydroxy compound until a saturated l~ solution is obtained. The dichloride precipitates from the solution during the process of saturation with hydrogen chloride gas. The l~ crystalline precipitate is collected and repeatedly washed with 16 water and then dried, for example, under vacuum.
17 Compound 3, the tetramethyltetrahydronaphthalene, and compound 6, (i.e. pentamethyltetrahydronaphthalene, in Reaction 19 Scheme IA, are prepared by reacting the 1~ 5 ~7 l 2,5-dichloro-2,5-dimethylhexane compound with benzene and tol-2 uene, respectively under Friedel-Crafts conditions. For example, 3 the 2,5-dichloro- material is dissolved in benzene which has been 4 cooled to between about -10 and 10C. Approximately a 50%
~ molar excess of anhydrous aluminum chloride relative to the 6 2,5-dichloro- material is added. After addition of the anhydrous 7 aluminum chloride, the mixture is stirred at between about 10 and 50C, preferably at room temperature, for between 1 and 6 hours, 9 preferably 3 hours. The solution is then refluxed for about 30 minutes to 2 hours, but preferably approximately 1 hour. The ~ resulting solution is acidified and the product recovered by 12 extraction and other means such as fractional distillation.
3 The ketones of formula 4 or 7 in Scheme IA are obtained by treating the corresponding tetrahydronaphthalene with acetyl chloride in the presence of aluminum chloride. A suspension of 16 aluminum chloride in a polar inert solvent is prepared under an 7 inert atmosphere and at reduced temperature, i.e., -10 to 10C.
The inert atmosphere may be argon or nitrogen, preferably argon.
~g The reaction is conveniently carried out in a solvent such as x methylene chloride. To the aluminum chloride suspension is added the tetrahydronaphthalene and acetyl chloride via a dropping funnel or similar device. About a 5% molar excess of acetyl chloride and 10% molar excess of aluminum chloride, 2. relative to the tetrahydronaphthalene material, is used. The ~ reaction is effected with agitation (stirring) over 0.5-4 hours at a !j 26 temperature between 10-50C. Preferably the reaction is effected 27 in about 2 hours at room temperature. Then the reaction is ;;
quenched with water and/or ice, the product extracted and further purified by distillation or some other appropriate means.
30 The carboxylic acid functlon (formulas 5 ~ 8) made by " ~ .

.
:3 ,.~

~. i .~ . ~ . . .- ' . .. . . .. .
. ~ - - . . . ~ .. .. . .

^ 133~7 ~ oxidizing the ketone with some oxidant such as a hypohalite salt or 2 acid dichromate oxidant. Preferably the oxidant will be a 3 hypohalite salt and the reaction will be carried out in the presence of a dilute base with a water-miscible organic solvent such as an ether. For example aqueous sodium hypochlorite in a four-fold 6 excess or more, is mixed with dilute base such as 2N NaOH in dioxane along with the acetyl-substituted tetrohydronaphthalene.
~ This mixture is heated at between about room temperature and 9 100 degrees for 30 minutes to 4 hours, preferably about 2 hours.
A pot temperature of 60-70 degrees will effect the oxidation in .
ll this time period. After discarding the organic layer, a reducing 12 agent is added to remove any residual oxidant. The solution is 13 then acidified with a strong acid such as sulfuric acid and the tetrahydronaphthoic acid removed by conventional means.
l~ Treating this acid, or its analogues, with the appropriate 16 phenol or thiophenol gives compounds of formula I. Most means 17 for esterification or thioesterification will provide the desired l~ compounds of formula I. In these cases, esterification was 19 effected by treating the appropriate acid and phenol with 1,3-dicyclohexylcarbodiimide and 4-dimethylaminopyridine.
If the Z group is an alcohol, aldehyde or ketone, it can first be protected before being used in the foregoing coupling reaction.
Alcohols may be protected as ethers or esters, and aldeh~des and ketones as acetals or ketals by known methods such as those described in M~Omie. Plenum Publishing Press, 1973 and ~ Protectin~ Groul~s. Ed. Greene, John Wiley & Sons, 1981. These 1 same procedures can be used to make ethers, acetals and ketals at some other point in the synthetic process.
As regards Reaction Scheme II, the starting material, 30 1-bromo-3-phenylpropane, is readily available from any fine ~ 16639 "

. ' ~
: . '.":`'~ , ~". , ': ' ' ' ', ' ., ' 133~

1~

~ chemical house. Conversion of the primary bromide to the tertiary 2 alcohol, formula 9, is effected by a Grignard type reaction using 3 magnesium, dry solvent such as dry diethyl ether and acetone.
4 The magnesium is first introduced into a dry flask under an inert atmosphere (eg. nitrogen) with dry solvent. The bromo compound 6 iS then added under the inert atmosphere with heat to cause 7 refluxing for a short period, 5 to 45 minutes. Then an appropriate ~ amount of acetone is added under a dry, inert atmosphere. Heat is 9 then applied to cause refluxing for about 10 to 60 minutes. Water, which can be in the form of ice, is then added, and the compound ll purified by standard techniques.
12 Ring closure (formula 10) is effected by treating the tertiary 13 alcohol with acid, preferably a strong acid like sulfuric acid, at reduced temperature, eg. -10 to +10C. After a brief reaction ~' time, the reaction product is recovered by extraction steps 16 commonly used in the art. The resulting 17 1,1-dimethyl-1,2,3,4-tetrahydronaphthalene is then converted to the two acids, 8,8-dialkyl acid and the 5,5-dialkyl acid, by the 19 steps outlined above under Reaction Scheme I. ~
~ Preparation of compounds with the reverse connectivity, that ~ -21 is where A is -OC(O)-, is illustrated in Reaction Scheme III. The ~
phenol, or a corresponding 2-alkyl substituted phenol, is reacted -with a tetrahydrofuran in the presence of aluminum chloride (Priedel-Crafts reaction). An alkane or similar type solvent is used. The reaction is effected first at room temperature for up to ~
i 26 5 hours, preferably about 2.5 hours, then at reflux for about an - -equal period of time. A dilute soluton of acid (eg. 3N HCI) is then added to quench the reaction. Normal isolation techniques are then used to recover the compound.
30 Terephthallic acids, the acids of Reaction Scheme III, are , ;l .
.~ .
' ' :

I ~' ' ' ~' ' ~3~67 l readily available from most chemical supply houses. They may be 2 esterified and selectively hydrolyzed to the mono-acid. The 3 coupling reaction used to make the final product is the same or an obvious variation of the generalized reaction sequence and ~ conditions given for Reaction Scheme I.
6 Alcohols are made by converting the corresponding acids of 7 formula I to the acid chloride with thionyl chloride (J. March, "Advanced Organic Chemistry", 2nd Edition, McGraw-Hill Book 9 Company), then reducing the acid chloride with sodium borohydride (March, Ibid, pg. 1124), or by diborane reduction.
Alternatively, aldehydes of formula II can be reduced tO the alcohol using sodium borohydride.
13 Aldehydes of formula III compounds can be prepared from the corresponding primary alcohols using mild oxidizing agents ' such as exemplified by pyridinium dichromate in methylene 16 chloride (Corey, E.J., Schmidt, G., Tet. Lett.. 399, 1979~. Alkylating 17 these alcohols with appropriate alkyl halides under Williamson reaction conditions (March, Ibid, pg. 357) gives the corresponding 19 ethers.
Acetals can be prepared from the corresponding aldehyde by the method described in March, Ibid, p 810.
Example 1 2.5-Dichloro-2.$-dimethylhexane 2~ Hydrogen chloride gas was bubbled through a suspension of ~ 48g (0.33 mol) of 2,S-dimethyl-2,5-hexanediol (Aldrich) in 600 ml 26 of concentrated HCI until the solution was saturated. The resultant Z7 crystalline product was collected by filtration, washed repeatedly with water and dried on a vacuum line to give the title compound ~9 as a white crystalline material. PMR (CDC13): w 1.60 (12H, s), 1.94 30 (4H, s).

. ~ .

. . .

.

. .. ~;.~.. ~ ~. . . ..
... ~. .` .. .

2 Exam~le 2 3 1.1,4,4-Tetramethyl-1.2.3.4-tetrahydronaphthalen~
A vigorously stirred solution of 100g (0.55 mol) ~ 2,5-dichloro-2,5-dimethylhexane in 300 ml of benzene was cooled 6 in an ice bath and treated with 45g (0.34 mol) anhydrous 7 aluminum chloride in small portions. This mixture was stirred at ~ room temperature for 3 hours, refluxed for 1 hour, cooled and 9 poured into a mixture of ice and HCI. The organic layer was ~o separated and the aqueous layer extracted with ether. Organic fractions were combined, washed with water, saturated Na2(~
~2 saturated NaCI solution and then dried (MgSO4). After removal of ~3 solvent, the residue was fractionally distilled (78C, 0.8 mm) to give the captioned compound as a colorless liquid. PMR (CDC13): w 1.3 (12H, s), 1.7 (4H, s), 7.1 (2H, m), 7.5 (2H, m).
~6 ~ ~ ~
~7 Exam~le 3 ",5.5.8.8-Tetramethyl-2-acetyl-5.6.7.8-tetrahydrona~hthalene ~9 A suspension of 3.45g (25.9 mmol) aluminum chloride in ~ ~ ~
x 15 ml methylene chloride was cooled under argon in an ice-salt ~;
2. bath and treated with stirring with a mixture of 4g (21.2 mmol) ~ ;~
1,1,4,4-tetramethyl-1,2,3,4-tetrahydronaphthalene and 1.94g (24.7 mmol) acetyl chloride via a dropping funnel over a period of thirty minutes. The cooling bath was removed and the mixture stirred for 2 hours, then quenched with ice. The organic layer was separated and the aqueous layer extracted with 2 x 50 ml methylene chloride. Organic extracts were combined and washed with water and saturated NaHCO3 solution and then dried D (MgSO4). Solvent was removed in-vacuo and the residue distilled x by the kugelrohr method (90C; 0.45 mm) to give the title J

. ~

- 133~

l compound as a colorless oil. PMR (CDC13): w 1.32 (6H, s), 1.33 ~6H, 2 S), 1.72 (4H, s), 2.60 (3H, s), 7.41 (lH, d, J N 8.9 Hz), 7.71 (lH, dd, J
3 N 8.8, 2.6 Hz) 7.96 (lH, d, J N 2.6 Hz).
,.
~ Example 4 6 5.5.8.8-Tetramethyl-5.6.7.8-tetrahydro-2-naphthoic acid 7 A mixture of 3.8g (16.5 mmol) of 5,5,8,8-tetramethyl-~ 2-acetyl-5,6,7,8-tetrahydronaphthalene from the preceeding g Example 3, 70 ml of 5.25% aqueous sodium hypochlorite (49 mmol), 25 ml of aqueous 2N NaOH and 30 ml of dioxane was heated at 60-70C for 2 hours. The mixture was allowed to cool and the oily organic layer removed. Then the aqueous layer was 3 washed with two portions of ether. The aqueous layer was then treated with sodium metabisulfite solution until the solution was negative to the potassium iodide/starch test. The aqueous layer 16 was then cooled and acidified with H2SO4. The resultant white ~ precipitate was collected by filtration and washed with water.
18 This crude product was further purified by recrystallization from 9 an ethanol/water mixture to give the title compound as a white, crystalline solid. PMR (CDC13): w 1.31 (6H, s), 1.32 (6H, s), 1.71 2~ (4H, s), 7.40 (lH, d, J N 8.8 Hz), 7.85 (lH, dd, J N 8.8 Hz, 1.8 Hz), 8.08 (lH, d, J N 1.8 Hz).

'~ Example S
Preparation of 4-Substituted Phenolic Esters A. pentadeuteroethyl 4-hydroxybenzoate - A mixture of 2.6552 g (19.2238 mmol) of 4-hydroxybenzoic acid, 1 g (19.1864 mmol) of hexadeuteroethanol, 20 ml of benzene and 5 drops of concentrated H2SO4 was heated at reflux for 24 hours on an 30 apparatus fitted with a Dean-Stark trap. The solvent was removed .
,~

;
., , -, :, ,, ,`.'~
,~ . ~
.... . . . ..

I' 1 3 3 ~

~ and the residue extracted with ether. The ether extract was 2 washed with water, saturated NaHCO3 a~d saturated NaCI
3 solutions and then dried (MgS04~. Solution was filtered and 4 concentrated in-vacuo. The residue was purified by flash 5 chromatography (silica; 15% ethyl acetate in hexanes) to give the 6 title compound as a white solid. PMR (CDC13): 6.84 (2H, d, 7 JN8.8 Hz), 7.95 (2H, d, JN8.8 Hz). ~3~ -~ Using the same general procedure, but using n-hexanol g instead, n-hexyl 4-hydroxybenzoate was synthesized as a colorless, viscous oil. PMR (CDC13): w 0.92 (3H, m), 1.36 (6H, m), 1l 1.78 (2H, m~, 4.33 (2H, q, JN6.7 Hz), 6.97 (2H, d, JN8.8 Hz), 7.99 12 (2H, d, JN8.8 Hz).
3 B. n-Tetrade~L4-hydroxyberlz~o~te~ - To a solution of 2.76 g (20 mmol) of 4-hydroxybenzoic acid and 800 mg ~200 mmol) of ~ sodium hydroxide in 12 ml of water was added 250 mg of 16 methyl tricaprylammonium chloride and 4.67 g (17 mmol) of 7 n-tetradecylbromide. The mixture was heated at reflux for 4 h and then diluted with 30 ml of water. The mixture was extracted 9 with 2x30 ml ether. The ether extracts were combined and washed with water and saturated NaCl solution. The solvent was removed in-vacuo and the residue purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a white solid. PMR (CDC13): w 0.88 (3H, m), 1.26 (20H, broad s), 1.42 (2H, m), 1.75 (2H, m), 4.29 (2H, t, JN6.6 Hz), ~ 6.90 (2H, d, JN8.8 Hz), 7.96 (2H, d, JN8.8 Hz).
26 C Tert-butvl 4-hydroxybenzoate - Excess isobutylene gas 27 was condensed at -78C in a high-pressure tube containing 13.8 g a (0.1 mol) of 4-hydroxybenzoic acid dissolved in 50 ml of dioxane ~ and 1 ml of conc. H2SO4 was then added to the mixture. The tube 30 was then sealed and the reaction mixture warmed to room .~", , ~ , 1 ~ 6 ~
.
.

I temperature and stirred for 2 hours. The mixture was then cooled 2 to -78C and the tube was opened and its contents poured slowly 3 into an excess of saturated NaHCO3 solution. Any excess ;~
isobutylene was removed by means of a nitrogen stream and the ~ mixture was extracted with ether. The ether solution was 6 extracted with lN NaOH solutisn and the ether layer was 7 discarded. The aqueous extract was acidified with dilute H2SO4 ~ and then extracted with ether. The ether extract was washed with 9 NaHCO3 solution and then dried (Na2SO4). The solution was filtered and the solvent removed in-vacuo. The residue was purified by flash chromatography (silica; 40% ethyl acetate in 1~ hexanes) to give the title compound as a white solid. PMR (CDC13):
13 w 1.59 (9H, s), 6.90 (2H, d, JN8.5 Hz), 7.89 (2H, d, 14 JN8.5 Hz), 8.0 (1H, broad s).
~5 n. Ethyl 4-hydro~-3-methylbenzoate - Ethyl 16 4-amino-3-methylbenzoate (3.85 g; 21.5 mmol) was dissolved in hot, 35% H2SO4/water and the mixture then cooled to below 5C.
An ice-cold solution of 1.91 g (22.5 mmol) of sodium nitrite in 9 20 ml of water was then slowly added to the mixture such that the temperature of the mixture never exceeded 5C. The mixture was stirred at 5C for 10 minutes and then treated with I g of urea and stirred for a further 10 minutes. A solution of 50 g (207 mmol) of cupric nitrate trihydrate in 750 ml of water was added to the reaction mixture followed by 2.87 g of cupr~us oxide. The mixture was stirred for a further 15 minutes and then extracted with 3x300 ml ether. The ether extracts were ~ combined and then washed with water and saturated NaCI solution 3 and then dried (MgSO4). The solution was filtered, the solvent removed in-vacuo and the residue purified by flash 30 chromatography (silica; 13% ethyl acetate in hexanes to 2~% ethyl i ~ ... ........ .. - .. ~

. , . ~ .

. . . ~ .

~33~7 t 21 ~
., .

l acetate in hexanes) to give the title compound as a pale yellow 2 solid. PMR (CDC13): w 1.39 (3H, t, JN7.1 Hz~, 2.28 (3H, s), 3 4.37 (2H, q, JN7.1 Hz), 6.87 (lH, d, JN8.5 Hz), 7.38 4 (lH, s), 7.79 (lH, dd, JN8.5 Hz, 2.0 Hz), 7.85 (lH, d, 5 JN2.0 Hz).
6 E. Ethyl 4-hydroxy-3~5-dimethylbenzoate - A mixture of ~
7 500 mg (3 mmol) of 4-hydroxy-3,5-dimethylbenzoic acid, 20 ml -~ of absolute ethanol and a catalytic amount of anhydrous HCI was 9 heated at reflux for 2 h. The mixture was then poured into excess cold water and the resultant precipitate was filtered. The precipitate was washed with water and dried in-vacuo to give the 1~ title compound as a white solid. PMR (CDC13): w 1.38 (3H, t, 13 JN7.0 Hz), 2.27 (6H, s), 4.33 (2H, q, JN7.0 Hz), 5.30 (lH, broad s), u 7.70 (2H, s).
15 F. 4-Tert-butyldimethylsiloxvmethvlphenol - A mixture of 16 1.24g (0.01 mole) of 4-hydroxymethylphenol, 1.8g (0.012 mole) of 17 tert-butyldimethylsilyl chloride, 1.7g (0.025 mole) of imidazole 1- and 3 ml of dimethylformamide was stirred under nitrogen at 19 room temperature for 12h. The reaction mixture was poured into 20 water and extracted with three portions of ether. Ether e~tracts were combined and washed successively with water and saturated NaCl solution and then dried (Na2SO4). The ether solution was concentrated in-vacuo and the resultant crude product was purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a colorless oil. PMR (CDC13):
26 w 0.09 (6H, s), 0.93 (9H, s), 4.66 (2H, s), 5.69 (lH, broad s), 6.74 D (2H, d, J N 6.9 Hz), 7.16 (2H, d, J N 6.9 Hz).
G. 4-Dimethoxymethylphenol - A mixture of 4.88 g (40 ~ mmol) of 4-hydroxybenzaldehyde, 6.6 g (206 mmol) of methanol 30 and 5.1 g (48 mmol) of trimethylorthoformate and 28 mg of :

,~
3 ~
: ~
-: ;~
',~ ~;~",-~

~ p-toluene sulfonic acid was stirred at room temperature for 12 h.
2 An excess of NaHCO3 was then added and the mixture stirred for a 3 further 60 h. The mixture was then filtered, the solvent removed 4 in-vacuo and the residue purified by flash chromatography (silica;
~ 20% ethyl acetate in hexanes) to give the title compound as a 6 viscous oil. PMR (CDC13): w 3.26 (6H, s), 5.38 (lH, s), 6.82 (2H, d, 7 JN8.5 Hz), 7.31 (2H, d, JN8.5 Hz), 7.36 (lH, broad s). ~;

9 Example 6 ~o Ethvl 4-(5.S.8.8-tetramethyl-S.6.7.8-tetrahydro-2-11 naphthovloxv!benzoate ~2 A solution of 116 mg (O.S mmol) of 5,5,8,8-tetramethyl-13 5,6,7,8-tetrahydro-2-naphthoic acid, 58 mg (O.S mmol) of ethyl 4-hydroxybenzoate, 117 mg (0.56 mmol) of ~ 1,3-dicyclohexylcarbodiimide and 30 mg (0.25 mmol) of 16 4-dimethylaminopyridine in lS ml of methylene chloride was stirred at room temperature for 12 hours. The reaction mixture was then filtered and the filtrate concentrated in-vacuo. The ~9 resultant residue was purified by flash chromatography (silica; 5%
ethyl acetate in hexanes) to give the title compound as white crystals. PMR (CDC13): w 1.32 (6H, s), 1.36 (6H, s), 1.42 (3H, t, JN7.0 Hz), 1.73 (4H, s), 4.40 (2H, q, JN7.0 Hz), 7.28 (2H, d, JN8.1 Hz), 7.45 (lH, d, JN8.8 Hz), 7.93 (lH, dd, JN8.8 Hz, 1.8 Hz), 8.13 (2H, d, JN8.1 Hz), 8.14 (lH, s).
Using the same general procedure and materials, but 26 substituting the appropriate phenol for ethyl 4-hydroxybenzoate, the following compounds were synthesized:
A. Benzyl 4-(5.5.8~8-tetramethyl-5.6.7.8-tetrahvdro-2-naphthovloxy)benzoate - Using benzyl 4-hydroxybenzoate, the 30 title compound was synthesized as a white, crystalline solid. PMR

~,.,~

r ~ ' ~

133~7 ~ (CDC13): w 1.32 (6H, s), 1.35 (6H, s), 1.72 (4H, s), 5.38 (2H, s), 2 7.24-7.48 (8H, m), 7.92 (lH, dd, JN8.8 Hz, 1.8 Hzj, 8.12-8.20 (3H, 3 m)-B. ~entadeuteroethyl 4-(5.5.8.8-tetramethyl-5.6.7.8-5 tetrahydro-2-naphthoyloxy!benzoate - Using pentadeuteroethyl 6 4-hydroxybenzoate, the captioned compound was synthesized as a 7 colorless oil. PMR (CDC13): w 1.33 (6H, s), 1.36 (6H, s), 1.73 (4H, s), 7.30 (2H, d, JN8.7 Hz), 7.46 (lH, d, JN8.3 Hz), 7.96 (lH, dd, 9 JN8.3 Hz, 1.8 Hz), 8.15 (2H, d, JN8.7 Hz), 8.18 (lH, d, JNl.8 Hz).
~o C n-Hexvl 4-(5.5.8.8-tetramethyl-5.6.7.8-tetrahydro-2-~ hthoyloxy!benz~o~Q- Using n-hexyl 4-hydroxybenzoate, the ~2 title compound was synthesized as a colorless oil. PMR (CDC13): w 3 0.92 (3H, m), 1.33 (6H, s), 1.35 (6H, s), 1.42 (6H, m), 1.74 (4H, s), 4 1.77 (2H, m), 4.34 (2H, t, JN6.7 Hz), 7.30 (2H, d, JN8.8 Hz), 7.46 5 (lH, d, JN8.3 Hz)), 7.95 (lH, dd, JN8.3 Hz, 1.9 Hz), 8.14 (2H, d, 16 JN8.8 Hz), 8.17 (lH, d, JNl.9 Hz).
7 D. n-Tetradecvl 4-(5.5.8.8-tetramethvl-5.6.7.8-tetra-hydro-2-naphthoyloxy!benzoate - Using n-tetradecyl 9 4-hydroxybenzoate, the title compound was synthesized as a colorless oil. PMR (CDC13): w 0.83-0.94 (3H, m), 1.15-1.50 (34H, m), 1.70-1.85 (6H, m), 4.34 (2H, t, JN6.7 Hz), 7.29 (2H, d, JN8.7 Hz), 7.46 (lH, d, JN8.4 Hz), 7.95 (lH, dd, JN8.4 Hz, 1.8 Hz), 8.14 (2H, d, JN8.7 Hz), 8.16 (lH, d, JNl.8 Hz).
E. tert-Butyl 4-(5.5.8.8-tetramethyl-~.6.7.8-tetra-~ hydro-2-naphthoylo~y!benzoate - Using tert-butyl 26 4-hydroxybenzoate, the title compound was synthesized as a 27 white solid. PMR (CDC13): w 1.33 (6H, s), 1.35 (6H, s), 1.62 (9H, s), 1.73 (4H, s), 7.25 (2H, d, JN8.7 Hz), 7.45 (lH, d, JN8.4 Hz), 7.93 ~ (lH, dd, JN8.4 Hz, 1.8 Hz), 8.07 (2H, d, JN8.7 Hz), 8.15 (lH, d, 30 JNl.8 Hz)-~ ~3~7 1 F. Ethyl 4-(~,5.8.8-tetral?rlç~hyl-5.6,7.8-tetrahydro- ;
2 2-naphthoylQxv)-3-methylbenzoate - Using ethyl 3 4-hydroxy-3-methylbenzoate, the title compound was synthesized 4 as a white solid. PMR (CDC13): w 1.34 (6H, s), 1.36 (6H, s), 1.41 5 (3H, t, JN7.2 Hz), 1.74 (4H, s), 2.30 (3H, s), 4.39 (2H, t, JN7.2 Hz), 6 7.22 (lH, d, JN8.4 Hz), 7.47 (lH, d, JN8.3 Hz), 7.94-8.04 (3H, m), 7 8.19 (lH, d, JNl.7 Hz).
~ G. Ethyl 4-(5.5.8.8-tetra~nethyl-5.6.7.8-tetrahydJo-9 2-naphthoyloxvl-3.5-djmethylbenz~aIç - Using ethyl 4-hydroxy-3,5-dimethylbenzoate, the title compound was synthesized as a white solid. PMR (CDC13): w 1.37 12 (6H, s), 1.39 (6H, s), 1.44 (3H, t, JN7.0 Hz), 1.77 (4H, 13 S), 2.27 (6H, s), 4.41 (2H, q, JN7.0 Hz), 7.50 (lH, d, 14 JN8.4 Hz), 7.86 (2H, s), 8.03 (lH, dd, JN8.4 Hz, 2.0 15 Hz), 8.23 (lH, d, JN2.0 Hz).
16 H.
17 4-~5.5.8 8-Tetran~ethyl-$~6~7~X-tetrahvdro-2-rlaphth-ovloxy!b-l- enzamide - Using 4-hydroxybenzamide, the title 19 compound was synthesized as a white solid. PMR (CDC13):
w 1.35 (6H, s), 1.37 (6H, s), 1.76 (4H, s), 7.32 (2H, d, JN8.6 Hz), 7.48 (lH, d, JN8.4 Hz), 7.89-7.98 (3H, m), 8.17 (lH, d, JNl.9 Hz).
I. 4-Methoxymethyl~henyl 5.5.8.8-tetramethyl-5.6.7.8-tetrahydro-2-na~hthoate - Using 4-methoxymethylphenol, the title compound was synthesized as a colorless oil. PMR (CDC13):
26 w 1.36 (6H, s), 1.38 (6H, s), 1.76 (4H, s), 3.44 (3H, s), 4.52 (2H, s), 7.22 (2H, d, JN8.4 Hz), 7.43 (2H, d, JN8.4 Hz), 7.48 (lH, d, JN8.4 Hz), 7.97 (lH, dd, JN8.4 Hz, 1.5 Hz), 8.19 (lH, d, JNl.5 Hz).
J. 4-tert-butyldimethylsiloxvmethyl~henvl 5.5.8.8-30 tetramelhyl-5.6.7.8-tetrahydro-2-naphthoate Using ;~
,'", .'~ :

~ 3 3 ~
.

l 4-tert-butyldimethylsiloxymethylphenol, the title compound was 2 synthesized as a white solid. PMR (CDC13): w 0.14 (6H, s), 0.98 (9H, 3 S), 1.34 (6H, s), 1.37 (6H, s), 1.75 (4H, s), 4.79 (2H, s), 7.18 (2H, d, JN9.0 Hz), 7.40 (2H, d, JN9.0 Hz), 7.46 (lH, d, JN8.4 Hz), 7.88 (lH, dd, JN8.4 Hz, 1.7 Hz), 8.18 (lH, d, JNl.7 Hz).
6 K 4-Formy~henyl 5.5.8.8-tetra~ethy~-5.6.7.8-tetra-7 hydro-2-naphthoate - Using 4-hydroxybenzaldehyde, the title ~ compound was synthesized as a white solid. PMR (CDC13): w 1.32 9 (6H, s), 1.34 (6H, s), 1.73 (4H, s), 7.39 (2H, d, JN9.0 Hz), 7.45 (lH, d, JN8.4 Hz), 7.92-7.98 (3H, m), 8.16 (lH, d, JNl.8 Hz), 9.99 (lH, 11 s) . : .
12 L. 4-Acetvlphenvl 5~5.8.8-tetramethyl-5.6.7.8-tetra-13 hydro-2-naI)hthoate - Using 4-acetylphenol, the title compound was synthesized as a white solid. PMR (CDC13): w 1.36 (6H, s), 1.38 l~ (6H, s), 1.76 (4H, s), 2.64 (3H, s), 7.34 (2H, d, JN8.4 Hz), 7.48 (lH, 16 d, JN8.4 Hz), 7.98 (lH, dd, JN8.4 Hz, 2.4 Hz), 8.07 (2H, d, 17 JN8.4 Hz), 8.19 (lH, d, JN2.4 Hz).
- M. 4-Dimethoxymethvlphenyl-5.5.8.8-tetramethvl-19 5.6.7.8-tetrahydro-2-naphthQa~ - Using 4-dimethoxymethylphenol, the title compound was synthesized as a colorless oil. PMR (CDC13): w 1.32 (6H, s), 1.34 (6H, s), 1.72 (4H, s), 3.34 (6H, s), 5.44 (lH, s), 7.21 (2H, d, JN8.4 Hz), 7.44 (lH, d, JN8.4 Hz), 7.52 (2H, d, JN8.4 Hz), 7.94 (lH, dd, JN8.4 Hz, 1.8 Hz), 8.16 (lH, d, JNl.8 Hz).
N. 4-Ethoxyphenyl 5.5.8.8-tetramethyl-5.6.7.8-tetra-26 hvdro-2-na~hthoate - Using 4-ethoxyphenol, the title compound was synthesized as a white solid. PMR (CDC13): w 1.32 (6H, s), 1.34 (6H, s), 1.42 (3H, t, JN7.0 Hz), 1.72 (4H, s), 4.04 (2H, q, JN7.0 Hz), ~ 6.92 (2H, d, JN9.0 Hz), 7.10 (2H, d, JN9.0 Hz), 7.43 (lH, d, 30 JN8.3 Hz), 7.93 (lH, dd, JN8.3 Hz, 1.9 Hz), 8.15 (lH, d, JNl.9 Hz).

,;~

O. 4-Ben~vloxyphenyl 5.5,~18-tetramethyl-5.6.7.8-2 tetrahydro-2-r~hthoate - Using 4-benzyloxyphenol, the title 3 compound was synthesized as a white solid. PMR (CDC13): w 1.32 (6H, s), 1.34 (6H, s), 1.72 (4H, s), 5.07 (2H, s), 7.00 (2H, d, ~ JN9.3 Hz), 7.11 (2H, d, JN9.3 Hz), 7.31-7.47 (6H, m), 7.92 (lH, dd, 6 JN8.4 Hz, 1.9 Hz), 8.14 (lH, d, JNl.9 Hz).
7 P. p-Toluyl 5.5.8.8-tetramethvl-$.6.7.8-tetrahydrQ-2-naphthoate - Using p-cresol, the title compound was synthesized 9 as a white solid. PMR (CDC13): w 1.34 (6H, s), 1.36 (6H, s), 1.74 (4H, s), 2.39 (3H, s), 7.09 (2H, d, JN8.4 Hz), 7.23 ~2H, d, JN8.4 Hz), 7.45 (lH, d, JN8.3 Hz), 7.95 (lH, dd, JN8.3 Hz, 1.9 Hz), 8.17 (lH, d, 12 JNl.9 Hz).
13 Q. Phenyl 5.5.8.8-tetramethyl-5.6.7.8-tetrahydro-2-nayhthoate - Using phenol, the title compound was synthesized 1~ as a white solid. PMR (CDCL3): w 1.35 (6H, s), 1.38 (6H, s), 1.76 16 (4H, s), 7.21-7.32 (3H, m), 7.41-7.50 (3H, m), 7.99 (lH, dd, 17 JN8.5 Hz, 1.8 Hz), 8.21 (lH, d, JNl.8 Hz).
1~
Exam~1~7 4-(5.5.8.8-Tetramethyl-5.6.7.8-tetrahydro-2-naphthoyloxy!benzoic acid A mixture of 150 mg (0.3394 mmol) of benzyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoate and 50 mg of 10% palladium on carbon in 5 ml of ethyl acetate was stirred under a hydrogen atmosphere at room 26 temperature for 4 hours. The reaction mixture was then filtered n and the filtrate was concentrated in-vacuo. The residue was ~ dissolved in ether and extracted with aqueous NaOH solution. The 2g aqueous extract was then acidified with glacial acetic acid and 30 extracted with ether. The ether extract was washed with ~ saturated NaCl solution and then concentrated in-vacuo. The 2 resultant residue was recrystallized from ethyl acetate to give the 3 title compound as a white solid. PMR (CDC13): w 1.34 (6H, s), 1.36 (6H, s), 1.76 (4H, s), 7.33 (2H, d, J N 8.6 Hz), 7.46 (lH, d, J N 7.8 Hz), ~ 7.94 (lH, dd, J N 7.8 Hz, 1.8 Hz), 8.16 (lH, d, J N 1.8 Hz), 8.21 (2H, 6 d, J N 8.6 Hz).

Example 8 9 1.1.4.4.6-Pelltamethyl-1,2.3.4-tetrahydrona~hthalelle To a cooled (0C) mixture of 40g (0.4341 mol) toluene and 25g (0.195 mol) 2,2,5,5-tetramethyltetrahydrofuran was added in ~ ' 12 small portions with stirring 26.6g (0.2 mol) of anhydrous 3 aluminum chloride. The cooling bath was removed and the ~:
mixture stirred at room temperature for 20h and then heated at reflux for 2 hours. This mixture was allowed to cool to room 16 temperature and then the reaction quenched by pouring into a 7 mixture of ice and 100 ml 3N HCI. The organic layer was separated and the aqueous layer extracted with 3 x 75 ml ether.
9 The organic extracts were combined and washed with 3N HCl, saturated NaHCO3, saturated NaCI solution and dried (MgSO4).
Solvent was removed in-vacuo and the residue was fractionally distilled to give the captioned compound as a colorless oil. PMR
(CDC13): 1.30 (6H, s), 1.32 (6H, s), 1.70 (4H, s), 2.33 (3H, s), 6.98 (lH, d, J N 7 Hz), 7.14 (lH, s), 7.23 (lH, d, J N 7 Hz).
Example 9 2-Acetyl-3.5.5.8.8-pentamethyl-5.6.7.8-tetrahydronaphthalene z~ To a suspension of 13.72g (102.9 mmol) aluminum chloride in -40 ml dichloroethane, which was cooled in an ice-acetone bath ~ under argon, was added with stirring over lh a solution of 17.1 lg 30 (84.56 mmol) of 1,1,4,4,6-1 pentamethyl-1,2,3,4-tetrahydroDaphthtalene in 1\0 ml 2 dichloroethane. The cooling bath was removed ~D3~ the mix~
3 stirred at room temperature for 3 hou~s, then ~Di~rl~ed onto ir~
4 The organic layer was separated and the aqueilw~ yer ext~o~ia 5 with 3 x 75 ml methylene chlo~ide. The organis ~ers were 6 combined and washed several times wish wat~er, E~,t~rated 7 NaHC03, saturated NaCI solution and then dri~ $o4). $q~11wi~aa$
~ was removed in-vacuo and residue subjected lt~ 3~ 1rohr 9 distillation ~70~C, 0.15 mm) to give the caption~dl ~ampound :~s al low-melting yellow solid. PMR (CDC13): w 1.30 ~ s), 1.32 S~iiHl.t $.).
1.70 (4H, s), 2.51 (3H, s), 2.59 (3H, s), 7.16 (lH, s~7.69 (lH, $~
2ExamI~le 10 ~33.5.5.8.8-Pentamethvl-5~.7.8-tetrahvrlro-2-4naphthoic acid A mixture of 8.2g (0.0336 mol) of 16 2-acetyl-3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydrv- naphthal~
17 90 ml of l.l9M (0.107 mol) aqueous sodium hypochlorite an~
1- ml of dioxane was stirred at room temperature fDI 0.5 hours ~;31 19 at 60C for 2 hours. A further 70 ml of l.l9M (0.~833 mol) off aqueous sodium hypochlorite was then added to the reaction ~ mixture and the mixture stirred at 70~C for 1 hou~i~s. The rea~3n n mixture was then cooled and treated with aqueou$ sodium bisulfite solution until the mixture was negative it~ starch/io~læ
'~ paper. The mixture was washed with ether and thcn acidifie;dl with H2S04. The mixture was extracted with three portions 0 2' ethe~ and the ether extracts were then combined and washe~
2' successively with water and saturated NaCl solution and the~
dried (MgSO4). The ether solution was th~n coDcæntrated ain~a ~e title compound obtained ~s colorless crystals by ~crystalliza~
from cold ether. PMR ~ q3): w 1.29 (6H, s), 1.3~ (6H, s), 1.

:::
13~

(4H, s), 2.60 (3H, s), 7.17 (lH, s), 7.26 (lH, s~.
. .
3 Example 11 4 Ethvl 4-(3.5.5.8.8-~entamethyl-5.6.7.8-tetrahydro-2-naphthoyloxy~benzoate : ':
6 A mixture of 399.2 mg (1.6204 mmol) of 7 3,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoic acid, 271.8 ~ mg (1.6355 mmol) of ethyl 4-hydroxybenzoate, 336.6 mg (1.6339 9 mmol) of 1,3-dicyclohexylcarbodiimide and 44.5 mg (0.3642 mmol) of 4-dimethylaminopyridine in 20 ml of methylene chloride was stirred at room temperature for 23h. The reaction mixture was filtered and the residue washed with 25 ml of - ~ -3 methylene chloride. The filtrate was concentrated in-vacuo and 4 the resultant crude product was purified by flash chromatography ~' (silica; 10% ethyl acetate in hexanes) to give the title compound as 16 a white solid. PMR (CDC13): w 1.34 (6H, s), 1.36 (6H, s), 1.43 (3H, t, 7 J N 7.2 Hz), 1.74 (4H, s), 2.66 (3H~ s), 4.42 (2H, q, J N 7.2 Hz), 7.26 (lH, s), 7.31 (2H, d, J N 8.7 Hz), 8.16 (2H, d, J N 8.7 Hz), 8.17 (lH, s).
19 Using the same general procedure and using instead benzyl 4-hydroxybenzoate, benzyl 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate was synthesized as a colorless oil. PMR (CDC13: w 1.32 (6H, s), 1.35 (6H, s), 1.72 (4H, s), 2.63 (3H, s), 5.39 (2H, s), 7.24 (lH, s), 7.29 (2H, d, J N 8.4 Hz), 7.34 - 7.49 (5H, m), 8.14 (lH, s), 8.18 (2H, d, J N 8.4 Hz).
Using the same general procedure but using instead ~ 4-methoxymethylphenol, 4-methoxymethylphenyl 3,5,5,8,8-Z7 pentamethyl-5,6,7,8-tetrahydro-2-naphthoate was synthesized as a colorless oil. PMR (CDC13): w 1.34 (6H, s), 1.37 (6H, s), 1.74 (4H, ~ s), 2.66 (3H, s), 3.43 (3H, s), 4.52 (2H, s), 7.21 (lH, s), 7.22 (2H, d, -30 JN8.3 Hz), 7.26 (lH, s), 7.43 (2h, d, JN8.3 Hz), 8.17 (lH, s).

"~r., ... ... . . . . . . .

13305~7 Example 12 34-(3.5.5.8.8-Pentamethyl-5.6.7.8-tetrahydro-2-naphthoyloxy!benzoic acid A mixture of 430 mg (0.94 mmol) of benzyl 6 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-be-7 nzoate, 60 mg of 10% palladium on carbon and 6 ml of ethyl ' acetate was stirred under a hydrogen atmosphere at room g temperature for 3 hours. A further 6 ml of ethyl acetate was then added to the reaction mixture and mixture heated at 50C for 3 hours. The reaction mixture was then cooled, filtered through 12 celite*and the residue washed with 5 ml of warm ethyl asetate.
3 The filtrate was then concentrated in-~acuo and the resultant ~ residue recrystallized from a mixture of ethyl acetate and hexanes J' to give the title compound as a white, crystalline solid. PMR
16 (CDC13): w 1.32 (6H, s), 1.34 (6H, s), 1.72 (4H, s), 2.62 (3H, s), 7.24 (lH, s), 7.32 (2H, d, J N 8.2 Hz), 8.13 (lH, s), 8.20 (2H, d, J N 8.2 Hz).
,.
9 Example 13 ,2-Me,thvl-5-phenvl-2-pentanol A mixture of 8.8 g. (0.37 mol.) of magnesium turnings and ~ lS0 ml of dry ether was placed in a 3-necked flask fitted with a a nitrogen inlet, a reflux condenser and an addition funnel containing 73.7 g (0.37 mol) of 1-bromo-3-phenylpropane. A
small amount of the bromo compound was added to the reaction ~5 mixture and the mixture warmed in order to initiate reaction. The D reaction mixture was treated with lS0 ml of dry ether and then the bromo compound was added at such a rate as to maintain ~ gentle reflux. The reaction mixture was heated at reflux for a ' further lS minutes and then treated slowly with 21.5 g * Trade-mark ~
.

~ 3 ~ 7 I (0.37 mol) of acetone. The mixture was heated at reflux for a 2 further 30 minutes, cooled and then poured slowly into 300 g of 3 crushed ice. The resultant white precipitate was dissolved by the addition of 20% H2SO4. The organic layer was separated and the ~ aqueous layer extracted with ether. The organic extracts were 6 combined and washed with water and saturated NaCl solution and 7 then dried (MgSO4). The solution was filtered and the solvent ~ removed in-vacuo. The residue was distilled (120C; 6 mm) to 5 give the captioned compound as a colorless oil. PMR (CDC13~: w 1.18 (6H, s), 1.44-1.53 (2H, m), 1.62-1.72 (2H, m), 2.61 (2H, t, JN7.6 Hz), 7.16^7.30 (5H, m).
1~ . .
13 E2~amI~le 14 Dimethvl-1.2.3.4-tetrahvdronaphthalene To 18 ml of ice-cold concentrated H2SO4 was added 17.8 g ~6 (0.l mol) of 2-methyl-5-phenyl-2-pentanol over 10 minutes. The 7 mixture was then stirred at 0C for 15 minutes and at room temperature for 15 minutes. The mixture was treated with 9 50 ml of water and then extracted with ether. The ether extracts ~ ~ - ~ were combined and washed with water and saturated NaCI and D NaHCO3 solutions and then dried (MgS04). The solution was filtered and the solvent removed in-vacuo. The residue was purified by distillation (93C; 10 mm) to give the title compound as a colorless oil. PMR (CDC13): w 1.19 (6H, s), 1.45-1.53 (2H, m), ~ 1.62-1.73 (2H, m), 2.62 (2H, t, JN6.1 Hz), 7.14-7.30 (4H, m).
26Example 15 272-f 1-hydroxyethyl!-8.8-dimethyl-5.6.7.8-tetrahvdro-naphthalene and 2-(1-hydroxyethyl!-5.5-dimethyl-5.6.7.8-tetrahydronaphthalene 30A solution of 4.0 g (25 mmol) of 1,1-dimethyl-1,2,3,4-~t,: . : . . . . .
~''""`''' :'',' ;~ . ' , '': ,: , ' ' .~ ... - . ~ - . . . ... .

133~

~ tetrahydronaphthalene and 2.35 g (30 mmol) of acetyl chloride in 2 5 ml of methylene chloride was added slowly to a stirred 3 suspension of 4.27 g (32 mmol) of anhydrous aluminum chloride in 15 ml of methylene chloride at 0C. After approximately half the solution had been added, the cooling bath was removed and 6 the addition completed at room temperature. The reaction 7 mixture was then stirred for 1 hour and poured into 70 ml of ~ ice-water mixture. The organic layer was separated and washed 9 successively with dilute HCI, water and saturated NaCl solution and then dried (MgSO4). The solution was filtered and the solvent removed in-vacuo and the residue distilled (100C; 0.1 mm) to 12 give an approximately 2:1 mixture of the ketones, 3 2-acetyl-8,8-dimethyl-5,6,7,8- tetrahydronaphthalene and 2-acetyl-5,5-dimethyl- 5,6,7,8-tetrahydronaphthalene, as a colorless oil.
16 A solution of 4.0 g (19.8 mmol) of the mixture of ketones, D prepared above, in 10 ml of dry ether was added slowly to a stirred mixture of 250 mg (6.7 mmol) of lithium aluminum - hydride in 30 ml of dry ether. The reaction mixture was heated at reflux for 0.5 h and then cooled and the excess lithium aluminum hydride destroyed by the careful addition of ethyl acetate. Water was then added to the mixture followed by sufficient dilute HCl to dissolve any precipitate. The organic layer was separated and washed successively with water and saturated NaCl solution and then dried (MgSO4). The solution was filtered and the solvent 2~ removed in-vacuo. The residue was purified by distillation (115C; 1 mm) followed by high pressure liquid chromatography (Whatman M20 Partisil*column; 10% ethyl acetate in hexanes;
~ 9.9 ml/min) to give the pure title compounds as colorless viscous 3~ oils.
* Trade-mark ;~

~ ~ 3 ~

PMR (CDC13) for 2-(1-hydroxyethyl)-8,8-dimethyl-2 5,6,7,8-tetrahydronaphthalene: w 1.28 (3H, s), 1.29 (3H, s), 1.47 3 (3H, d, JN6.6 Hz), 1.61-1.70 (2H, m), 1.72-1.83 (2H, m), 2.75 (2H, t, JN6.3 Hz), 4.82 (lH, q, JN6.6 Hz), 7.02 (lH, d, JN7.8 Hz), 7.08 (lH, ~ dd, JN7.8 Hz, 1.8 Hz), 7.32 (lH, d, JNl.8 Hz).
6 PMR(CDC13) for 2-(1-hydroxyethyl)-5,5-dimethyl-7 5,6,7,8-tetrahydronaphthalene: w 1.28 (6H, s), 1.47 (3H, d, ~ JN6.6 Hz), 1.60-1.68 (2H, m), 1.72-1.83 (2H, m), 2.74 (2H, t, 9 JN6.4 Hz), 4.78 (lH, q, JN6.6 Hz), 7.03 (lH, d, JNl.8 Hz), 7.11 (lH, dd, JN8.1 Hz, 1.8 Hz), 7.29 (lH, d, JN8.1 Hz).

1~ Example 16 13 2-Acetyl-8.8-dimethyl-5.6.7.8-tetrahydronaphthalene To a stirred solution of 2.44 g (11.96 mmol) of ~s 2-(1-hydroxyethyl)-8,8-dimethyl-5,6,7,8-tetrahydro- naphthalene 16 in 35 ml of methylene chloride was added 6.75 g (17.9 mmol) of 17 pyridinium dichromate and 330 mg (1.68 mmol) of pyridinium -~
1- trifluoroacetate. The mixture was stirred at room temperature for 19 24 h and then diluted with 35 ml of low-boiling petroleum ether.
3 The mixture was filtered through a short column of anhydrous 2~ MgSO4 and silica and the filtrate then concentrated in-vacuo to give the title compound as a colorless oil. PMR (CDC13): w 1.30 (6H, s), 1.60-1.70 (2H, m), 1.72-1.84 (2H, m), 2.56 (3H, s), 2.78 (2H, t, JN6.1 Hz), 7.08 (lH, d, JN7.8 Hz), 7.61 (lH, dd, JN7.8 Hz, 1.9 Hz), ~ 7.93 (lH, d, JNl.9 Hz).
2C Using the samc general procedure, but using instead 2- (1 -hydroxyethyl)-5,5-dimethyl-5,6,7,8-tetrahydro- naphtha-lene, the ketone, 2-acetyl-5,5-dimethyl-5,6,7,8-~ tetrahydronaphthalene was synthesized as a colorless s~il. PMR
x (CDC13): w 1.29 (6H, s), 1.64-1.70 (2H, m), 1.76-1.87 (2H, m), 2.55 . .~. ~, . . . : : . .

i.~.

-~3~

l (3H, s), 2.81 (2H, t, JN6.1 Hz), 7.40 (lH, d, JN8.4 Hz), 7.64 (lH, d,2 JNl.8 Hz), 7.71 (lH, dd, JN8.4 Hz, 1.8 Hz).

Exam~le 17 8.8-Dimethyl-5.6.7.8-tetrahydro-2-naphthoic acid 6 A mixture of 1.0 g (4.95 mmol) of 7 2-acetyl-8,8-dimethyl-5,6,7,8-tetrahydronaphthalene, 1.8 g of ~ sodium hydroxide, 62 ml of 10% sodium hypochlorite solution, 10 9 ml of water and lS ml of dioxane was heated at 65C until thin layer chromatography analysis (silica; 10% ethyl acetate in hexanes) indicated absence of starting ketone. The mixture was ~2 cooled to room temperature and sodium metabisulphite added 3 until solution was negative to starch-iodide paper. The mixture was then acidified (pH = 4) with dilute H2SO4 and the resultant 15 precipitate was filtered, washed with water and dried under 16 vacuum to give the captioned compound as a white solid. PMR
~7 (CDCl3): w 1.32 (6H, s), 1.64-1.72 (2H, m), 1.78-1.88 (2H, m), 2.82 ~8 (2H, t, JN6.1 Hz), 7.14 (lH, d, JN8.4 Hz), 7.80 (lH, dd, JN8.4 Hz, 19 1.8 Hz), 8.10 (lH, d, JNl.8 Hz). ~ y,~O
Using the same general procedure, but using instead 2-acetyl-S,S-dimethyl-5,6,7,8-tetrahydronaphthalene, the acid, S,S-dimethyl-5,6,7,8-tetrahydro-2-naphthoic acid was synthesized as a white solid. PMR (CDC13): w 1.30 (6H, s), 1.64-1.71 (2H, m), 1.75-1.84 (2H, m), 2.81 (2H, t, JN6.1 Hz), 7.40 (lH, d, JN8.3 Hz), 7.81 (lH, d, JNl.8 Hz), 7.85 (lH, dd, JN8.3 Hz, 1.8 Hz).
Exam~le 18 z~ F~thvl4-(8.8-dimethyl-s.6.7.8-tetrahydro-2-naphth benzoate A solution of 220.7 mg (1.0804 mmol) of 8,8-dimethyl-' 5,6,7,8-tetrahydro-2-naphthoic acid, 180.6 mg (1.0868 mmol) of ~ ~3~6~

I ethyl 4-hydroxybenzoate, 227.3 mg (1.1034 mmol) of 2 1,3-dicyclohexylcarbodiimide and 22.9 mg (0.1874 mmol) of 3 4-dimethylaminopyridine in 15 ml of methylene chloride was stirred at room temperature for 18 h. The reaction mixture was ~ then filtered and the residue washed with 10 ml of methylene 6 chloride. The filtrate was concentrated in-vacuo and the resultant 7 crude product purified by flash chromatography (silica; 5% ethyl acetate in hexanes) to give the title compound as a colorless oil.
9 PMR (CDC13): w 1.35 (6H, s), 1.42 (3H, t, JN7.2 Hz), 1.68-1.76 (2H, to m), 1.80-1.92 (2H, m), 2.85 (2H, t, JN6.1 Hz), 4.40 (2H, q, JN7.2 Hz), 7.18 (lH, d, JN8.0 Hz), 7.31 (2H, d, JN8.7 Hz), 7.89 (lH, 12 dd, JN8.0 Hz, 1.6 Hz), 8.11-8.22 (3H, m).
13 Using the same general procedure, but using benzyl 14 4-hydroxybenzoate instead, benzyl 4-(8,8-dimethyl-5,6,7,8-' tetrahydro-2-naphthoyloxy)benzoate was synthesized, a colorless 16 oil. PMR (CDC13): w 1.36 (6H, s3, 1.68-1.77 (2H, m), 1.80-1.92 (2H, 17 m), 2.86 (2H, t, JN6.3 Hz), 5.40 (2H, s), 7.19 (lH, d, JN8.0 Hz), - 7.29-7.51 (7H, m), 7.90 (lH, d, JN8.0 Hz), 8.15-8.23 (3H, m).
9 Using the same general procedure, but using instead 5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoic acid and ethyl 4-hydroxybenzoate, ethyl 4-(5,5-dimethyl-5,6,7,8-tetra-hydro-2-naphthoyloxy)benzoate was synthesized as a colorless oil.
PMR (CDC13): w 1.33 (6H, s), 1.41 (3H, t, JN7.2 Hz), 1.68-1.76 (2H, m), 1.80-1.90 (2H, m), 2.85 (2H, t, JN6.3 Hz), 4.39 (2H, q, JN7.2 Hz), 7.28 (2H, d, JN8.7 Hz), 7.47 (lH, d, JN8.4 Hz), 7.90 (lH, s), 7.94 25 (lH, d, JN8.4 Hz), 8.13 (2H, d, JN8.7 Hz).
21 Using the same general proce~ure, but using instead 5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoic acid and benzyl ~ 4-hydroxybenzoate, benzyl 4-(5,5-dimethyl-5,6,7,8-30 tetrahydro-2-naphthoyloxy)benzoate was synthesized, as a white `

I solid. PMR (CDC13): w 1.37 (6H, s), 1.71-1.78 (2H, m), 1.82-1.92 2 (2H, m), 2.88 (2H, t, JN6.3 Hz), 5.42 (2H, s), 7.33 (2H, d, JN8.7 Hz), 3 7.37-7.53(5H, m), 7.95 (lH, s), 7.99 (lH, d, JN8.4 Hz), 8.20 (2H, d, JN8.7 Hz).
Exam~le 19 64-(8.8-DimethyL-i~ 8-teltr~ a~hthoyloxy)-7benzoic acid A mixture of 120 mg (0.29 mmol) of benzyl 9 4-(8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoate, S0 mg of 10% palladium on activated carbon and 3 ml of ethyl acetate was stirred under a hydrogen atmosphere a~ room 12 temperature for 2 hour. The mixture was then centrifuged and t3 the supernatant solution decanted. The solvent was then removed in-vacuo and the residue recrystallized from ethyl acetate to give 5 the captioned compound as white crystals. PMR (CDC13): w 1.34 16 (6H, s), 1.67-1.75 (2H, m), 1.78-1.90 (2H, m), 2.85 (2H, t, 17 JN6.0 Hz), 7.18 (lH, d, JN8.1 Hz), 7.34 (2H, d, JN8.7 Hz), 7.88 (lH, 1- dd, JN8.1 Hz, 1.8 Hz), 8.16 (lH, d, JNl.8 Hz), 8.20 (2H, d, 19 JN8.7 Hz). Using the same general procedure, but using benzyl ~ 4-(S,S-dimethyl- 5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoate 21 instead, 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-~ benzoic acid was synthesized as white crystals. PMR (CDC13): w a 1.33 (6H, s), 1.67-1.74 (2H, m), 1.78-1.89 (2H, m), 2.86 (2H, t, JN6.3 Hz), 7.33 (2H, d, JN8.8 Hz), 7.47 (lH, d, JN8.1 Hz), 7.90 (lH, d, JNl.8 Hz), 7.95 (lH, dd, JN8.1 Hz, 1.8 Hz), 8;20 (2H, d, JN8.8 Hz).
Example 2Q
SJ~ 8-Tetramethyl-5,6.7.8-tetrahydro-2-naphtbol To a stirred solution of 13.2g (0.1403 mol) of phenol and 12.8g (0.0998 mol) of 2,2,5,5-tetramethyltetra-~" ~

133~

1 hydrofuran in 50 ml of heptane was added 13.1g (0.0982 mol) of 2 aluminum chloride in small portions. After the addition was 3 complete the mixture was stirred at room temperature for 2.5 4 hours, at reflux for 2 hours and then at room temperature for a 5 further 16 hours. The reaction mixture was then treated with 100 6 ml of 3N HCI and stirred for 0.5 hours. The mixture was filtered 7 and the residue washed with water and dried in-vacuo to give ~ crude product. The organic layer was separated from the filtrate 9 and the aqueous layer extracted with 3 x 75 ml of ether. The organic layers were combined and washed with saturated NaCl solution, dried (MgS04) and then concentrated in-vacuo to give further crude product. The crude product was recrystallized from 13 hexanes to give the title compound as pale brown crystals. PMR
(CDC13): w 1.26 (6H, s), 1.28 (6H, s), 1.67 (4H, s), 5.08 (lH, broad s), 5 6.68 (lH, dd, J N 8.7 Hz, 2.7 Hz), 6.82 (lH, d, J N 2.7 Hz), 7.16 (lH, 16 d, J N 8.7 Hz).
~7 Example 21 - Diethyl terephthalate 9 Hydrochloric acid gas was bubbled through 100 ml of absolute ethanol until the increase in weight of the ethanol was approximately Sg. Terephthalic acid, 16.6g (0.1 mol), was then added to the acidified ethanol and the mixture heated at reflux for ~ 31 hours. The reaction mixture was cooled, then filtered and the 2- residue washed with ethanol. The filtrate was concentrated in-vacuo and then poured into a mixture of water and 100 ml 26 ether. After extraction, the ether layer was separated and washed successively with water and saturated NaHCO3 solution and then dried (MgSO4). The ether solution was filtered and the solvent ~ removed in-vacuo to give the title compound as a white solid.
30 PMR (CDC13): w 1.42 (6H, t, 1 N 7.0 Hz), 4.40 (4H, q, J N 7.0 Hz), 8.10 ' ~330~7 I (4H, s).
2 Example 22 3 Ethvl hvdro~çnterephthalate 4 Anhydrous barium hydroxide (3.83g, 0.022 mol), W2S placed in a Soxhlet extractor and continuously extracted for 10 hours 6 with hot ethanol into a refluxing mixture of lOg (0.045 mol) of 7 diethyl terephthalate in 100 ml of absolute ethanol. The resultant ~ white precipitate was filtered and then washed with ethanol. The g precipitate was suspended in 100 ml ether and treated with excess dilute HCI. After extraction, the ether layer was separated and washed successively with water and saturated NaCI solution 12 and then dried (MgS04). The ether solution was filtered and the 13 solvent removed in-vacuo. The resultant residue was 14 recrystallized from acetonitrile to give the title compound as a 1~ white solid. PMR (CDC13): w 1.40 (3H, t, J N 7.0 Hz), 4.40 (2H, q, J N
16 7.0 Hz), 8.10 (4H, s), 9.1 (lH, broad s).
~7 Example 23 ~ enzyl tere~hthalate ~9 A mixture of 48.S (0.25 mol) of dimethylterephthalate, 108g (1.0 mol) of benzyl alcohol and O.5g of potssium tert-butoxide was prepared in S00 ml, 3-necked round bottom flask fitted with a ~ magnetic stir bar, a thermometer, a nitrogen inlet and an air a condenser. The stirred mixture was heated at 140C for 15 hours while a rapid stream of nitrogen was passed over the surface of -~ the mixture. Most of the excess benzyl alcohol was then removed --26 from the mixture by fractional distillation. The residue was dissolved in a mixture of ether and methylene chloride and silica was then added to the solution. The solution was then filtered and the solvent removed in-vacuo. The residual crude product was ~ ~ ~
30 recrystallized from a mixture of hexanes and tert-butyl methyl ~ `

1 6639 ~

it.
,r~ .

~ ' ~ ether to give the title compound as colorless crystals. PMR (CDC13):
2 w 5.38 (4H, s), 7.35 - 7.50 (lOH, m), 8.13 (4H, s).

4 Example 24 Benzyl hvdrogelltere~hthalate 6 To a heated mixture of 9.1g (26 mmol) of dibenzyl terephthalate in 90 ml acetone and 30 ml water was added ~ dropwise a solution of 1.05g (25 mmol) of lithium hydroxide 9 monohydrate in 10 ml of water and 10 ml of acetone. The reaction mixture was heated at reflux for a further 30 minutes with vigorous stirring. The reaction mixture was allowed to cool 12 and the aqueous solution was extracted with 2 x 10 ml of ether.
~3 The aqueous layer was then acidified with glacial acetic acid and 14 the resultant white precipitate extracted with 3 x 25 ml of ether.
I~ The ether extracts were combined, washed successively with 16 water and saturated NaCI solution and then dried (MgS04). The ether solution was then filtered and the solvent removed in-vacuo.
- The resultant residue was recrystallized from a mixture of acetone and water to give the captioned material as colorless crystals.
PMR (CDC13): w 5.40 (2H, s), 7.36 - 7.49 (SH, m), 8.18 (4H, s).
Example 25 Ethyl (5.5.8.8-tetramethyl-5.6.7.8-tetrahvdro-2-naphthvl!terephthalate ~' A solution of 598.8 mg (2.9308 mmol) 5,5,8,8-~ tetramethyl-5,6,7,8-tetrahydro-2-naphthol, 542 mg (2.7912 -26 mmol) of ethyl hydrogenterephthalate, 608 mg (2.9515 mmol) of 1,3-dicyclohexylcarbodiimide and 127 mg (1.0395 mmol) of 4-dimethylaminopyridine in 30 ml of methylene chloride was stirred at room temperature for 22h. The reaction mixture was 30 filtered and the residue washed with 10 ml of methylene chloride.

.. ;~: : ~ :: . , , ~- .,: : ~ . . . . .

1 3 r~

Y-~
~ The filtrate was concentrated in-vacuo and the resultant crude 2 product purified by flash chromatography (silica; 6% ethyl acetate 3 in hexanes) giving the captioned material as a white solid. PMR
~ (CDC13): w 1.32 (6H, s), 1.33 (6H, s), 1.46 (3H, t, JN 7.2 Hz), 1.73 5 (4H, s), 4.46 (2H, q, JN 7.2 Hz)r 7.02 (lH, dd, J N 8.5 Hz, 2.5 Hz), 6 7.14 (lH, d, JN 2.5 Hz), 7.38 (lH, d, JN 8.5 Hz), 8.19 (2H, d, JN8.1 7 Hz), 8.29 (2H, d, JN8.1 Hz).
Using the same general procedure, but using benzyl hydrogenterephthalate instead, benzyl (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)-terephthallate was synthesized as a white solid. PMR (CDC13): w 1.32 (6H, s), 1.33 (6H, s), 1.74 (4H, s), 5.44 (2H, s), 7.03 (lH, dd, JN 8.7 Hz, 2.4 Hz), 7.16 13 (lH, d, JN 2.4 Hz), 7.37 - 7.54 (6H, m), 8.23 (2H, d, J N 8.7 Hz), 8.30 14 (2H, d, J N 8.7 Hz).
.~
16Example 26 "(5.5.8.8-tetramethyl-5.6.7.8-tetrahydro-~-na~hthyl!hydrogentere~hthalate 9A mixture of 400 mg (0.9 mmol) of benzyl (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)- terephtha-2~ late, 60 mg of 10% palladium on carbon and 5 ml of ethyl acetate was stirred under a hydrogen atmosphere at room temperature for 3 hours. The reaction mixture was filtered and the filtrate evaporated to dryness in-vacuo to give the title compound as a white solid. PMR (CDC13): w 1.30 (12H, s), 1.71 (4H, s), 7.05 (lH, ~ dd, J N 9.0 Hz, 2.7 Hz), 7.12 (lH, d, J N 2.7 Hz), 7.36 (lH, d, JN9.0 2~ Hz), 8.25 (2H, d, JN 8.4 Hz), 8.31 (2H, d, JN8.4Hz).

Exam~le 27 30 Preferably, these compounds will be administered topically ~ 4.~

~ 3 ~

using various formulations. Two formulation are given as 2 examples here.

In~redient Weight/Percent 6 ~Qh~QIL
7 Retinoid 0.1 3 BHT 0.1 g Alcohol USP 58.0 : .
Polyethylene Glycol 400 NF 41.8 ,Gel 13 Retinoid 0.1 1- BHT 0.1 u Alcohol USP 97.8 Hydroxypropyl Cellulosc 2.0 ~ ~, /~ ~ . ~ ,~ ' .. ,...... :

Claims (18)

1. A compound of the formula where the R groups are independently hydrogen, or lower alkyl; A
is -C(O)O-, -OC(O)-, -C(O)S-, or -SC(O)-; n is 0-5; and Z is H, -COB
where B is -OH or a pharmaceutically acceptable salt, or B is -OR1 where R1 is an ester-forming group, or B is -N(R)2 where R is hydrogen or lower alkyl, or Z is -OE where E is hydrogen or an ether-forming group or -COR2 where R2 is hydrogen, lower alkyl, phenyl or lower alkyl phenyl, or Z is -CHO or an acetal derivative thereof, or Z is -COR3 where R3 is -(CH2)mCH3 where m is 0-4 and the sum of n and m does not exceed 4.

2. A compound of claim 1 where A is -C(O)O-; n is 0-1; Z is -COOH or a lower alkyl ester or amide or a pharmaceutically acceptable salt thereof, or -OH or an ester or ether thereof, or -CHO
is an acetal thereof.

3. A compound of claim 2 which is ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate.

4. A compound of claim 2 which is 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoic acid or a pharmaceutically acceptable salt thereof.

5. A compound of claim 2 which is 4-methoxymethylphenyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoate or 4-dimethyoxymethylphenyl-5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoate.

6. A compound of claim 2 which is 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzamide.

7. A compound of claim 2 which is 4-(8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoic acid or a pharmaceutically acceptable salt thereof, ethyl 4-(8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate, or benzyl 4-(8,8-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate.

8. A compound of claim 2 which is 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-benzoic acid or a pharmaceutically acceptble salt thereof, ethyl 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate, or benzyl 4-(5,5-dimethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate.

9. A compound of claim 1 where A is -C(O)O-; n is 0-1; the position-3 R group is lower alkyl; Z is -COOH or a lower alkyl ester or amide or a pharmaceutically acceptable salt thereof, -OH or an ester or ether derivative thereof, or -CHO or an acetal derivative thereof.

10. A compound of claim 9 which is 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)-be-nzoic acid or a pharmaceutically acceptable salt thereof.

11. A compound of claim 9 which is ethyl 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate.

12. A compound of claim 9 which is benzyl 4-(3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoyloxy)benzoate.

13. A compound of claim 9 which is 4-methoxymethylphenyl 3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoate or 4-formylphenyl 3,5,5,8,8-pentamethyl-5,6,7,8-tetrahydro-2-naphthoate.

14. A compound of claim 1 where A is -OC(O)-; n is 0-1; Z is -COOH or a lower alkyl ester or amide or a pharmaceutically acceptable salt thereof, or -OH or an ester or ether thereof or -CHO
or an acetal thereof.

15. A compound of claim 14 which is ethyl 4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)-ter-ephthalate.

16. A compound of claim 14 which is (5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-2-naphthyl)-hydrogenterephthalate.

17. The use of a compound according to claim 1, administered alone or in conjunction with a pharmaceutically acceptable excipient, for treating psoriasis in a mammal.

18. A pharmaceutical composition comprising a pharmaceutically acceptable excipient and a therapeutically effective amount compound of the formula according to claim 1.