CA1266438A - Therapeutic application of n-substituted 2- aminomethylene-1,3-indanediones - Google Patents
Therapeutic application of n-substituted 2- aminomethylene-1,3-indanedionesInfo
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- CA1266438A CA1266438A CA000486914A CA486914A CA1266438A CA 1266438 A CA1266438 A CA 1266438A CA 000486914 A CA000486914 A CA 000486914A CA 486914 A CA486914 A CA 486914A CA 1266438 A CA1266438 A CA 1266438A
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/10—Antioedematous agents; Diuretics
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Abstract
ABSTRACT OF THE DISCLOSURE
The present invention to pharmaceutical composition comprising an effective amount of products having the structural formula (I) where R1 is a hydrogen atom or a lower alkyl group such as methyl or ethyl, R2 is a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or lower alkyl group from C1 to C4 such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl; the NR1R2 group can also represent a nitrogenous heterocyclic compound N(CH2)n in which n can be any value between 4 and 6.
The products are useful in human and veterinary therapy because of their anti-inflammatory, diuretic, bronchodilating, anticholinergic, antispasmodic and antidepressant properties.
The present invention to pharmaceutical composition comprising an effective amount of products having the structural formula (I) where R1 is a hydrogen atom or a lower alkyl group such as methyl or ethyl, R2 is a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or lower alkyl group from C1 to C4 such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl; the NR1R2 group can also represent a nitrogenous heterocyclic compound N(CH2)n in which n can be any value between 4 and 6.
The products are useful in human and veterinary therapy because of their anti-inflammatory, diuretic, bronchodilating, anticholinergic, antispasmodic and antidepressant properties.
Description
:~6643~3 TITLE OF THE INVENTION
THERAPEUTIC APPLICATION OF N-SUBSTITUTED
THERAPEUTIC APPLICATION OF N-SUBSTITUTED
2-AMINOMETHYLENE-1,3-INDANEDIONES
BACKGROUND OF THE INVENTION
Field of the Invention:
The present invention relates to N-substituted 2-aminomethylene-1,3~indanediones and their therapeutic application.
Discussion of the Background:
The present invention relates to prod~cts having the structural formula ~ ~ CH - NR~R2 (I) in which Rl is a hydrogen atom or a Cl_6 group, such as, for example, methyl or ethyl, R2 is a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or Cl_4 alkyl group, such as, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl; the NRlR2 group can ~1~
~6643~3 also represent a nitrogenous heterocyclic compound N(CH2)n, in w~ich n can be 4, 5 or 6.
The products of the above structural form~la have been previously described in the l:iterature. Studies reported by Gasjuna, L. et al. in Latv. P.S.R. Zinat.
Akad. Vest. Kim. Ser., 1980, 1:98-L01, can be cited by way of example. ~owever, no therapeutic application has been described for these derivatives.
There is a strongly felt need in the medical art for compounds possessing good pharmacological properties. For example, products having anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic and antidepressant properties are much needed in medicine.
SUMMARY OF THE INVENTION
Accordingly, it is an object of this invention to provide a novel pharmaceutical composition.
It is another object of this invention to provide a novel pharmacological composition which possesses anti-inflammatory propertiesO
It is another object of this invention to provide a novel pharmacological composition which possesses diuretic properties.
It is another object of this invention to provide a pharmacological composition possessing bronchial dilating properties.
~iG~3~
It is another object of this invention to provide a novel pharmacological composition w~ich possesses anticholinergic properties.
It is another object of -this invention to provide a novel pharmacological composition which possesses antispasmodic properties.
It is another object of this invention to provide a novel pharmacological composition which possesses antidepressan-t properties.
It is another object of this invention to provide a novel pharmacological composition which possesses anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic or antidepressant properties and which may be used in human or veterinary therapy.
In is another object of this invention to provide a novel anti-inflammatory treatment which comprises administering an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel diuretic treatment which comprises administering an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel bronchial dilatin~ treatment which comprises the administration of an effective amount of the novel pharmaceutical composition of this invention.
~LZ66~38 It is another object of this invention to provide a novel anticholinergic treatment which comprises the administration of an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel antispasmodic treatmen-t which comprises the administration of an eEfective amount: of the novel pnarmaceutical composition o~ this invention.
It is another object of this invention to provide a novel antidepressant treatment which comprises the administration of an effec~ive amount of t'ne novel pharmaceutical composition of the present invention.
Applicants have surprisingly discovered that each and every one of the above objects of this invention have been satisfied with a novel pharmacological composition containlng (1) a pharmaceutically acceptable excipient, and (2) an effective amount of at least one product having the structural formula O
~ ~ ~ =CH - NR1R2 (I) in which Rl is a hydrogen atom or a Cl_6 alkyl group, such as methyl or ethyl;
~Z6~ 3l3 R2 is a straight or branched cyclopropylmethyl, 2-furyl. methyl, benzyl, phenyl or Cl_4 alkyl group such as, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, and tertiary butyl, the NRlR2 group can also be a nitrogenous heterocyclic compound 1, N(CH2)n, wherein n may be 4, 5 or 6.
The inventors have now discovered that the products according to the formula (I) exhibit pharmacological properties, viz~ of an anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic and-antidepressant nature, which allows them to be used in human and veterinary therapy.
The present invention thus relates to a novel pharmacological composition which comprises (1) a pharmaceutically acceptable excipient, and (2) an effective amount of at least one product having the following structural formula ~ ~ =CH - NR1R2 (I) ~266~3~
where Rl is a hydrogen atom or a Cl_6 alXyl group, such as methyl or ethyl; and R2 is a straight or branched cyclopropylmethyl, ~-furyl methyl, benzyl, phenyl or a Cl_4 alkyl group, such as, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, or tertiary butyl; and the NRlR2 group can also be a nitrogenous heterocyclic compound N(CH2)n, where n can be 4, 5 or 6.
In a preferred embodiment of this invention the novel pharmacological composition is useful for the treatment of edema or arterial hypertension.
In another preferred embodiment of this invention, the novel pharmaceutical composition i5 useful for the treatment of spasmodic condition.
In another preferred embodiment, the novel pharmaceutical composition is useful as a psychotropic drug in the treatment of depressions.
In anot'ner preferred embodiment, the novel pharmaceutical composition is useful for the treatment of asthmatic conditions.
The novel pharmaceutical composition of this invention is characterized by the fact that it contains an effective amount of at least one product of formula I in combination with a pharmaceutical or veterinary vehicle or appropriate excipient.
The products of the present invention are generally prepared by a reaction which involves 2-formyl-1,3-indanedione and an amine of the formula HNRlR2~ in which Rl represents a hydrogen a-tom or a Cl_6 alkyl group, such as methyl or ethyl: R2 represents a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or a Cl_4 alkyl group, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, or tertiary butyl. The NRlR2 group can also represent a nitrogeneous heterocyclic compound N(CH2)n, w~ere n may be 4, 5 or 6.
A variation of the preparation of these compounds consists of reacting 2-formyl-1,3-indanedione and the hydrochloride of the HNR1~2 amine defined above in the presence of a hydracid acceptor, such as sodium carbonate.
Other featues of the invention will become apparent in the course of the following descriptions of exemplary embodiments w~ich are given for illustration of the invention and are not intended to limiting thereof.
Example I
2-Methylaminomethylene-1,3-indanedione. (Product of formula (I) in which Rl = H and R2 = CH3; code name COR3726.) ~6~3~3 Preparation A solution of 35 ml of ethyl orthoformate and 70 ml acetic anhydride is added to 25 g 1,3-indanedione. The mixture is heated to 80C for one hour. The solution is filtered and immediately cooled in an ice bath. A quantity of 130 ml of previously boiled water is added while shaking; the solution is monitored to ensure that the temperature remains at 10C, left to crystallize in the cold for ~ive hours, and then filtered. The yield is 67~. The precipitate is poured into 400 ml of boiling ethyl alcohol. The mixture is main-tained in reflux for fi~e minutes and then filtered into a previously heated flask. The solution contains 20 g 2-formyl-1,3-indanedione and must be used rapidly.
A solution of 1.2 g 2-formyl-1,3-indanedione in 50 ml ethyl alcohol is added to a methylamine solution in excess in 2 ml acetic acid and 50 ml ethyl alcohol. The yellow precipitate is filtered and washed in cold ethyl alcohol. The yield is 86%.
Physiochemical Properties Melting point: 254C (ethyl alcohol), sublimates.
Infrared spectrum: y(C0) bands at 1705 and 1650 cm~l.
NMR spectrum in DMS0 (d6): 9.5 ppm, singlet, 1 proton, NH; 8 ppm, singlet, 1 proton, CH; 7.73 ppm, ~Z~6~L3~3 multiplet, 4 protons, aromatic phthalyl hydrogen;
BACKGROUND OF THE INVENTION
Field of the Invention:
The present invention relates to N-substituted 2-aminomethylene-1,3~indanediones and their therapeutic application.
Discussion of the Background:
The present invention relates to prod~cts having the structural formula ~ ~ CH - NR~R2 (I) in which Rl is a hydrogen atom or a Cl_6 group, such as, for example, methyl or ethyl, R2 is a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or Cl_4 alkyl group, such as, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tertiary butyl; the NRlR2 group can ~1~
~6643~3 also represent a nitrogenous heterocyclic compound N(CH2)n, in w~ich n can be 4, 5 or 6.
The products of the above structural form~la have been previously described in the l:iterature. Studies reported by Gasjuna, L. et al. in Latv. P.S.R. Zinat.
Akad. Vest. Kim. Ser., 1980, 1:98-L01, can be cited by way of example. ~owever, no therapeutic application has been described for these derivatives.
There is a strongly felt need in the medical art for compounds possessing good pharmacological properties. For example, products having anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic and antidepressant properties are much needed in medicine.
SUMMARY OF THE INVENTION
Accordingly, it is an object of this invention to provide a novel pharmaceutical composition.
It is another object of this invention to provide a novel pharmacological composition which possesses anti-inflammatory propertiesO
It is another object of this invention to provide a novel pharmacological composition which possesses diuretic properties.
It is another object of this invention to provide a pharmacological composition possessing bronchial dilating properties.
~iG~3~
It is another object of this invention to provide a novel pharmacological composition w~ich possesses anticholinergic properties.
It is another object of -this invention to provide a novel pharmacological composition which possesses antispasmodic properties.
It is another object of this invention to provide a novel pharmacological composition which possesses antidepressan-t properties.
It is another object of this invention to provide a novel pharmacological composition which possesses anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic or antidepressant properties and which may be used in human or veterinary therapy.
In is another object of this invention to provide a novel anti-inflammatory treatment which comprises administering an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel diuretic treatment which comprises administering an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel bronchial dilatin~ treatment which comprises the administration of an effective amount of the novel pharmaceutical composition of this invention.
~LZ66~38 It is another object of this invention to provide a novel anticholinergic treatment which comprises the administration of an effective amount of the novel pharmaceutical composition of this invention.
It is another object of this invention to provide a novel antispasmodic treatmen-t which comprises the administration of an eEfective amount: of the novel pnarmaceutical composition o~ this invention.
It is another object of this invention to provide a novel antidepressant treatment which comprises the administration of an effec~ive amount of t'ne novel pharmaceutical composition of the present invention.
Applicants have surprisingly discovered that each and every one of the above objects of this invention have been satisfied with a novel pharmacological composition containlng (1) a pharmaceutically acceptable excipient, and (2) an effective amount of at least one product having the structural formula O
~ ~ ~ =CH - NR1R2 (I) in which Rl is a hydrogen atom or a Cl_6 alkyl group, such as methyl or ethyl;
~Z6~ 3l3 R2 is a straight or branched cyclopropylmethyl, 2-furyl. methyl, benzyl, phenyl or Cl_4 alkyl group such as, for example, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, and tertiary butyl, the NRlR2 group can also be a nitrogenous heterocyclic compound 1, N(CH2)n, wherein n may be 4, 5 or 6.
The inventors have now discovered that the products according to the formula (I) exhibit pharmacological properties, viz~ of an anti-inflammatory, diuretic, bronchial dilating, anticholinergic, antispasmodic and-antidepressant nature, which allows them to be used in human and veterinary therapy.
The present invention thus relates to a novel pharmacological composition which comprises (1) a pharmaceutically acceptable excipient, and (2) an effective amount of at least one product having the following structural formula ~ ~ =CH - NR1R2 (I) ~266~3~
where Rl is a hydrogen atom or a Cl_6 alXyl group, such as methyl or ethyl; and R2 is a straight or branched cyclopropylmethyl, ~-furyl methyl, benzyl, phenyl or a Cl_4 alkyl group, such as, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, or tertiary butyl; and the NRlR2 group can also be a nitrogenous heterocyclic compound N(CH2)n, where n can be 4, 5 or 6.
In a preferred embodiment of this invention the novel pharmacological composition is useful for the treatment of edema or arterial hypertension.
In another preferred embodiment of this invention, the novel pharmaceutical composition i5 useful for the treatment of spasmodic condition.
In another preferred embodiment, the novel pharmaceutical composition is useful as a psychotropic drug in the treatment of depressions.
In anot'ner preferred embodiment, the novel pharmaceutical composition is useful for the treatment of asthmatic conditions.
The novel pharmaceutical composition of this invention is characterized by the fact that it contains an effective amount of at least one product of formula I in combination with a pharmaceutical or veterinary vehicle or appropriate excipient.
The products of the present invention are generally prepared by a reaction which involves 2-formyl-1,3-indanedione and an amine of the formula HNRlR2~ in which Rl represents a hydrogen a-tom or a Cl_6 alkyl group, such as methyl or ethyl: R2 represents a straight or branched cyclopropylmethyl, 2-furyl methyl, benzyl, phenyl or a Cl_4 alkyl group, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, or tertiary butyl. The NRlR2 group can also represent a nitrogeneous heterocyclic compound N(CH2)n, w~ere n may be 4, 5 or 6.
A variation of the preparation of these compounds consists of reacting 2-formyl-1,3-indanedione and the hydrochloride of the HNR1~2 amine defined above in the presence of a hydracid acceptor, such as sodium carbonate.
Other featues of the invention will become apparent in the course of the following descriptions of exemplary embodiments w~ich are given for illustration of the invention and are not intended to limiting thereof.
Example I
2-Methylaminomethylene-1,3-indanedione. (Product of formula (I) in which Rl = H and R2 = CH3; code name COR3726.) ~6~3~3 Preparation A solution of 35 ml of ethyl orthoformate and 70 ml acetic anhydride is added to 25 g 1,3-indanedione. The mixture is heated to 80C for one hour. The solution is filtered and immediately cooled in an ice bath. A quantity of 130 ml of previously boiled water is added while shaking; the solution is monitored to ensure that the temperature remains at 10C, left to crystallize in the cold for ~ive hours, and then filtered. The yield is 67~. The precipitate is poured into 400 ml of boiling ethyl alcohol. The mixture is main-tained in reflux for fi~e minutes and then filtered into a previously heated flask. The solution contains 20 g 2-formyl-1,3-indanedione and must be used rapidly.
A solution of 1.2 g 2-formyl-1,3-indanedione in 50 ml ethyl alcohol is added to a methylamine solution in excess in 2 ml acetic acid and 50 ml ethyl alcohol. The yellow precipitate is filtered and washed in cold ethyl alcohol. The yield is 86%.
Physiochemical Properties Melting point: 254C (ethyl alcohol), sublimates.
Infrared spectrum: y(C0) bands at 1705 and 1650 cm~l.
NMR spectrum in DMS0 (d6): 9.5 ppm, singlet, 1 proton, NH; 8 ppm, singlet, 1 proton, CH; 7.73 ppm, ~Z~6~L3~3 multiplet, 4 protons, aromatic phthalyl hydrogen;
3.3 ppm, singlet, 3 protons, CH3.
Example II
2-Ethylaminomethylene-1,3-indanedione. Product of formula (I) in which R1 = ~ and R2 = C2H5; code name COR3755.
Preparation A quantity of 4 ml of a 70~ aqueous ethylamine solution is added to a solution of ~.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated slightly in a water bath for 15 minutes. After cooling, the product formed precipitates. It is recrystallized in ethyl alcohol. The yield is 86.7%.
Physiochemical Properties Melting point: 170~C (ethyl alcohol).
NMR spectrum in CDC13: 9.33 ppm, singlet, 1 proton, ~H; 8 ppm, singlet, 1 proton, CH; 7.75 ppm, multiplet, 4 protons, aromatic phthalyl hydride;
3.55 ppm, multiplet, 2 protons, CH2; 1.38 ppm, triplet, 3 protons, C~3-~xample III
2-Anilinomethylene-1,3-indanedione. Product of formula (I) in which Rl = H and R2 = C6~15; code name COR3756.
~6643~ I
--1 o -Preparation Three grams of aniline is added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated sl:ightly in a water bath for 20 minutes. After cooling, the product formed precipitates. It is recrystallized in ethyl alcohol.
The yield is 67.1%
Physiochemical Properties Melting point: 197C (ethyl alcohol).
NMR spectrum in CDC13: 11 ppm, multiplet, 1 proton, NH, 8.38 ppm, singlet, 1 proton, H at 4 on aniline; 8.13 ppm, singlet, 1 proton, CH; 7.77 ppm, I
multiplet, 4 protons, aromatic ,~hthalyl hydride;
7.38 ppm, multiplet, 4 protons, H at 2,3,5,6 on anlllne .
Example IV
2-Isobutylaminomethylene-1,3-indanedione. Product of formula (I) in which Rl = H and R2 = CH2CH(CH3)2, code name COR3754.
Pre~aration Three grams of isobutylamine is added to a solution of 2 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The The mixture is heated slightly in a water bath for 10 minutes. The ethyl alcohol is removed by evaporation and the desired product is recrystallized in ethyl alcohol. The yield is 56~.
3~
Physiochemical Properties Melting point: 149C (ethyl alcohol~.
NMR spectrum in CDC13 9.42 ppm, singlet, 1 proton, NH; 7~93 ppm, singlet, 1 proton, =CH;
7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 3.3 ppm, duplet, 2 protons, CH2; 1.98 ppm, multiplet, 1 proton, CH; 1.025 ppm, duplet, 6 protons, c~3.
Example V
2-Isopropylaminomethylene-1,3-indanedione.
Product of formu~a (I~ in which Rl = ~ and R2 =
CH(CH3)2; code name COR3762.
Preparation Two milliliters of isopropylamine is added to a solution of 2.7 g 2-formyl-1,3-indanedione in 60 ml ethyl alcohol. The mixture is heated in a water bath for 30 minutes, The ethyl alcohol is removed by evaporation and the desired product is recrystallized in an isopropyl ether/ethyl alcohol (9/1) mixture and then in ethyl alcohol. The yield is 60%.
Physiochemical Properties Melting point: 122C (ethyl alcohol).
NMR spectrum in CDC13: 9.3 ppm, singlet, 1 proton, ~H; 8.05 ppm, singlet, 1 proton, =CH;
7.83 ppm, multiplet, 4 protons, aromatic ,bhthalyl ~2~ 3~
hydride; 3.77 ppm, multiplet, 1 proton, CH; 1.41 ppm, doublet, 6 protons, CH3.
Example VI
2-Cyclopropylmethylaminomethylene-1,3-indanedione. Product of formula (I) in which Rl = H
and R2 = CH2CH-CH2; code name COR3757.
Preparation CH
Three grams of cyclopropylmethylamine hydrochloride and 2.9 g sodium carbonate are added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 30 minutes and then filtered in the presence o~
heat. After cooling, the product formed precipitates. It is recrystallizea in ethyl alcohol.
The yield is 43%.
Physiochemical Properties Melting point: 157C (ethyl alcohol).
NMR spectrum in CDC13: 9.47 ppm, singlet, 1 proton, ~H; 8 ppm, singlet, 1 proton, -CH; 7.78 ppm, multiplet, 4 protons, aromatic phthalyl hydride;
3.37 ppm, doublet, 2 protons, CH2; 1.1 ppm, multiplet, 1 proton, CH; 1.7 ppm, multiplet, 2 protons, cyclical CH2; 0.38 ppm, multiple, 2 protons, cyclical CH2.
;438 Example VII
2-(2-Furyl methylaminomethylene)-1,3-indanedione.
Product of ~ormula (I) in which Ul = H and R2 = ~2 code nama COR3758.
Preparation A quantity of 2.7 g 2-furyl methylamine is added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 20 minutes. It is subsequently filtered aEter cooling. The precipitate is recrystallized in dioxane. The yield is 40.4%.
Physiochemical Properties Melting point: 216C (dioxane).
NMR spectrum in CDC13: 9.38 ppm, singlet, 1 proton, ~H; 7.97 ppm, singlet, 1 proton, CH;
7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 7.5 ppm, multiplet, 1 proton, H at 5 on the furyl nucleus; 6.45 ppm, multiplet, 2 protons, H a~. 3 and 4 on the furyl nucleus; 4.67 ppm, singlet, 1 proton, CH2; 4.53 ppm, singlet, 1 proton, C~?-Example VIII
2-Piperidinomethylene-1,3-indanedione. Product of formula (I) in which NRlR2 = ~(CH2)5; code name COR3759.
3L;Z6~38 Preparation A quantity of 2.5 g plperidine i3 added to a solution of 2.4 g 2-Eormyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 20 minutes. It is subsequently filtered after cooling. The precipitate is recry~tallized in ethyl alcohol. The yield is 44~.
Physiochemical Properties Melting point: 167~C (ethyl alcohol).
NMR spectrum in CDC13: 7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 7.6 ppm, singlet, 1 proton, CH; 4.53 ppm, multiplet, 2 protons, CH2 at 2 or 6 on the piperidine nucleus; 3.67 ppm, multiplet, 2 protons, CH2 at 2 or 6 on the piperidine nucleus; 1.83 ppm, multiplet, 6 protons, CH2 at 3, 4 and S on the piperidine nucleus.
Example IX
2-Dimethylaminomethylene-1,3-indanedione. Pro~uct of formula (I) in which Rl - R2 = CH3; code name COR3761.
Pre~aration Five milliliters of a 25~ dimethylamine solution in ethyl alcohol is added to a solution of 2.7 g 2-formyl-1,3-indanedione in 60 ml ethyl aLcohol. The mixture is heated at approxi~ately 40C for four hours. The solvent i8 removed by evaporation. The precipitate i9 isolated, then recrystallized in a mixture o isopropyl ~ther/ethyl alcohol (8/2). The yiela is 58%.
PhysicochemicaL Properties Melting point: 138C (ethyl alcohol).
MNR spectrum in CDC13: 7.8 ppm, multiplet, 4 protons, aromatic p~thalyl hydride; 7.6 ppm, singlet, 1 proton, =CH; 3.93 ppm, singlet, 3 proton, CH3;
3.42 ppm, singlet, 3 protons, CH3.
Example X
l-Perhydroazepinyl-2-methylene-1,3-indanedione.
Product of formula (I) in w~ich NR1R2 = N(CH2)6; code name COR3790.
Preparation Three milliliters hexamethylenimine is added to a solution of 1.6 g 2-ormyl-1,3-indanedione in 40 ml ethyl aIcohol. The mixture is 'neated in a water bath form 60 minutes. The ethyl alcohol is partially evaporated. The residue i8 refrigerated for 12 hours. The precipitate is filtered and then purified by passing over a silica column using ethyl ether as the eluent. The yield is 43%.
Physicochemical Properties Melting point: 125C (ethyl alcohol).
IR spectrum: ~O bands at 1700 and 1650 cm-l NMR spectrum in CDC13: 7.78 pprn, multiplet, 4 protons, aromatic phthalyl ~ydride; 7.63 ppm, singlet, 1 proton, CH; 4.50 ppm, multiplet, 2 ~rotons, CH2 at 2 or 7 on the perhydroazepinyl nucleus; 3.67 ppm, multiple-t, 2 protons, CH2 at 3, 4, S and 6 on the perhydroazepinyl nucleus.
The results of the toxicological and pharmacological studies performed on the products according to the present invention are reported below.
Toxicity CoR3726, COR3754, COR3755, COR3756, CoR3757~
COR3758, COR3759, COR3751, and coR379o caused no deaths in mice in an oral dose of 300 mg/kg or an intraperitoneal dose of 200 mg/kg. When administered to mice orally, dissolved in 20% TWEEN*, COR3761 exhibited an LD50 of 520 (457-592~ mg/kg.
Pharmacolo~y Diuretic activity was determined in several experimental models. In rats subjected to excess water intake, CoR376 and COR3761, administered in an oral dose of 20 mg/kg, increased urinary sodium excretion by * Trademark , , ~6~
a factor of 4.4 and 3.5, respectively. Spironolactone adminis-tered under -the same conditions and in the same dose increased sodium excretion by 3.6. ~hen given orally to rats subjected to excess sodium chloride intake, COR3761 produced the following increments in volumetric urinary excretion measured at the sixth hour: 10~ in a dose oE 10 mg/kg, 42!.5% in a dose o~
20 mg/kg and 68.4% in a dose o~ 40 mg/kg. COR3761 was administered to rats subjected to excess water intake and volumetric urinary excretion and sodium and potassium elimination were measured over a period of six ~ours. These parameters were, respectively, -13%, +73~, +77% af-ter administration of 10 mg/kg; +9%, +241%, ~114~ after 20 mg/kg and -4%, +532~, +138% after 40 mg/kg. The sodium/potassium ratio which was 0.4 in the control animals was 0.47 at 10 mg/kg, 0.62 at 20 mg/kg and 1.48 at 40 mg/kg. In the course of another experiment, volumetric urniary excretion and sodium and potassium elimination were, respectively: +1%, +100%, +54% at 20 mg/kg; +10%, +313~, +69~ at 40 mg/kg and +16%, ~356~ and +89% at 60 mg/kg. The sodium/potassium ratio went from 0.43 in the control animals to 0.53 at 20 mg per kg, 1.02 at 40 mg/kg and 1.12 at j60 mg/kg.
Spasmolytic activity was determined in vitro by measurement of t~e e:Efect of the test product on ileum contractions in guinea pigs induced by transmural ~4~ 3~
-la-electric transmission in an oxygenated Krebs solution at 32aC. When used in a concentration of 0.5 mcg/ml, COR3754 and COR3759 in~ibited these contractions by 50%. Domperidone ex~ibits ~he same activity in a concentration of 1 mcg/ml~
Anti-inflammatory activity was determined in rats by measurement of in~ibition oE the edema induc~d by intraplantar injection oE 0.1 ml of a 1~ carragheenin suspension. The test products were administered orally one hour before the carragheenin injection and the determination was made three hours after injection.
Doses of 100 mg/kg COR3755 and COR3761 produced 3G% and 49~ in~ibition, respectively. Aspirin administered under the same conditions in a dose oE 150 mg/kg produced 40% inhibition o the ede~a.
Bronchodilating activity was determined in vitro by measuremsnt of the flow of Tyrode's solution through an isolated and perfused guinea pig lung which had been contracted by addition of 0.05 mcg/ml methacholine to the perfusion liquid. CoR3755, CoR3757, COR3759, COR3761, COR3762 and COR3790, which were used, respectively, in concentrations of 50, 100, 10, 10, 25 and 100 mcg/ml, increased the flow by 50~.
Amino~hylline produces t'nis same efEect in a concentration of 100 mcg/ml.
3~3 Anticholinergic activity was evaluated by measuremPnt of the cont~actions inauced by 0.1 mcg/ml acetylcholine ln isolated segments of guinea pig ileum. When used in concentrations of 100, 50, 10, 50, 10 and 25 mcg/ml, respectively, CoR3755~ COR3757, COR3761, COR3762 and C0~3790 produced an 80~ inhibition of these contractions.
Central anticholinergic activity was evaluated by measurement of inhibition, under the test product, of muscular tremors induced in mice by ~ubcutaneous injection of 0.5 mg/kg oxotremorine. The tremors are rated according to an index ranging from O to 6, one hour after intraperitoneal injection of the test product. An index of O indicates absence of tremor while 6 represents maximum tremor. COR3762 administered in a dose of 100 mg/kg resulted in an index of 3; imipramine, given under the same conditions in a dose of 25 mg/kg produced the same activity.
~ ntidepressant activity was determined in the test involving potentiation of yohimbine toxicity and in the test involving in~ibition of reserpine-induced ptosis.
One hour before oral administration of the test product, a non-lethal dose of yohimbine, i.e., 15 mg/kg-doses of COR3761 and COR3762 produced 80% and 100% mortality, respectively.
Mice were given an oral dose oE the test product ninety minute~s beEore intraperitoneal injection of 5 mg/kg dissolved reserpine. Ptosis was evaluated according to an index oE 0 to 6, ~here 0 signifies ptosis and ~ indicates absence of pto~is. Under the experimental conditions, COR3761 and COR3762 in doses of 200 and 50 mg/kg, respectively, produces respective ratings of 5 and 4.
In view oE their p~armacological activity, which is associated with low toxicity, the products of the present invention can be used in human or ve-terinary therapy.
~ len combined with -the conventional vehicles, they can e.g., be utilized in -the treatment of cardiac, renal or hepatic edema and arterial hypertension, in the -treatment of spasmodic symptoms, especially of the digestive and respiratory systems, in the treatment oE
asthma conditions or for depressive states.
When combined with the conventional vehicles, depending on the indication, they can be administered e.g., by the oral route in the form of dragees, tables, syrups, vials; rectally in the form of suppositories:
by -the intramuscular route or the intravenous route.
According to the indication and the subject, dodes administered range ~rom 1-100 mg/day given in one to six administrations orally, from 1-100 mg/day given in ~166~3~3 one or two admini~trations rectally and from 0.5-50 mg given by parenteral injection.
Obviously, numerous modificatiolls and variation~
of the present invention are possible in light to the above teaching.s. It is therefore to be understood that within the scope of the appended cla:ims, the inv~ntion may be practiced otherwise than as specifically described herein.
Example II
2-Ethylaminomethylene-1,3-indanedione. Product of formula (I) in which R1 = ~ and R2 = C2H5; code name COR3755.
Preparation A quantity of 4 ml of a 70~ aqueous ethylamine solution is added to a solution of ~.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated slightly in a water bath for 15 minutes. After cooling, the product formed precipitates. It is recrystallized in ethyl alcohol. The yield is 86.7%.
Physiochemical Properties Melting point: 170~C (ethyl alcohol).
NMR spectrum in CDC13: 9.33 ppm, singlet, 1 proton, ~H; 8 ppm, singlet, 1 proton, CH; 7.75 ppm, multiplet, 4 protons, aromatic phthalyl hydride;
3.55 ppm, multiplet, 2 protons, CH2; 1.38 ppm, triplet, 3 protons, C~3-~xample III
2-Anilinomethylene-1,3-indanedione. Product of formula (I) in which Rl = H and R2 = C6~15; code name COR3756.
~6643~ I
--1 o -Preparation Three grams of aniline is added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated sl:ightly in a water bath for 20 minutes. After cooling, the product formed precipitates. It is recrystallized in ethyl alcohol.
The yield is 67.1%
Physiochemical Properties Melting point: 197C (ethyl alcohol).
NMR spectrum in CDC13: 11 ppm, multiplet, 1 proton, NH, 8.38 ppm, singlet, 1 proton, H at 4 on aniline; 8.13 ppm, singlet, 1 proton, CH; 7.77 ppm, I
multiplet, 4 protons, aromatic ,~hthalyl hydride;
7.38 ppm, multiplet, 4 protons, H at 2,3,5,6 on anlllne .
Example IV
2-Isobutylaminomethylene-1,3-indanedione. Product of formula (I) in which Rl = H and R2 = CH2CH(CH3)2, code name COR3754.
Pre~aration Three grams of isobutylamine is added to a solution of 2 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The The mixture is heated slightly in a water bath for 10 minutes. The ethyl alcohol is removed by evaporation and the desired product is recrystallized in ethyl alcohol. The yield is 56~.
3~
Physiochemical Properties Melting point: 149C (ethyl alcohol~.
NMR spectrum in CDC13 9.42 ppm, singlet, 1 proton, NH; 7~93 ppm, singlet, 1 proton, =CH;
7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 3.3 ppm, duplet, 2 protons, CH2; 1.98 ppm, multiplet, 1 proton, CH; 1.025 ppm, duplet, 6 protons, c~3.
Example V
2-Isopropylaminomethylene-1,3-indanedione.
Product of formu~a (I~ in which Rl = ~ and R2 =
CH(CH3)2; code name COR3762.
Preparation Two milliliters of isopropylamine is added to a solution of 2.7 g 2-formyl-1,3-indanedione in 60 ml ethyl alcohol. The mixture is heated in a water bath for 30 minutes, The ethyl alcohol is removed by evaporation and the desired product is recrystallized in an isopropyl ether/ethyl alcohol (9/1) mixture and then in ethyl alcohol. The yield is 60%.
Physiochemical Properties Melting point: 122C (ethyl alcohol).
NMR spectrum in CDC13: 9.3 ppm, singlet, 1 proton, ~H; 8.05 ppm, singlet, 1 proton, =CH;
7.83 ppm, multiplet, 4 protons, aromatic ,bhthalyl ~2~ 3~
hydride; 3.77 ppm, multiplet, 1 proton, CH; 1.41 ppm, doublet, 6 protons, CH3.
Example VI
2-Cyclopropylmethylaminomethylene-1,3-indanedione. Product of formula (I) in which Rl = H
and R2 = CH2CH-CH2; code name COR3757.
Preparation CH
Three grams of cyclopropylmethylamine hydrochloride and 2.9 g sodium carbonate are added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 30 minutes and then filtered in the presence o~
heat. After cooling, the product formed precipitates. It is recrystallizea in ethyl alcohol.
The yield is 43%.
Physiochemical Properties Melting point: 157C (ethyl alcohol).
NMR spectrum in CDC13: 9.47 ppm, singlet, 1 proton, ~H; 8 ppm, singlet, 1 proton, -CH; 7.78 ppm, multiplet, 4 protons, aromatic phthalyl hydride;
3.37 ppm, doublet, 2 protons, CH2; 1.1 ppm, multiplet, 1 proton, CH; 1.7 ppm, multiplet, 2 protons, cyclical CH2; 0.38 ppm, multiple, 2 protons, cyclical CH2.
;438 Example VII
2-(2-Furyl methylaminomethylene)-1,3-indanedione.
Product of ~ormula (I) in which Ul = H and R2 = ~2 code nama COR3758.
Preparation A quantity of 2.7 g 2-furyl methylamine is added to a solution of 2.4 g 2-formyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 20 minutes. It is subsequently filtered aEter cooling. The precipitate is recrystallized in dioxane. The yield is 40.4%.
Physiochemical Properties Melting point: 216C (dioxane).
NMR spectrum in CDC13: 9.38 ppm, singlet, 1 proton, ~H; 7.97 ppm, singlet, 1 proton, CH;
7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 7.5 ppm, multiplet, 1 proton, H at 5 on the furyl nucleus; 6.45 ppm, multiplet, 2 protons, H a~. 3 and 4 on the furyl nucleus; 4.67 ppm, singlet, 1 proton, CH2; 4.53 ppm, singlet, 1 proton, C~?-Example VIII
2-Piperidinomethylene-1,3-indanedione. Product of formula (I) in which NRlR2 = ~(CH2)5; code name COR3759.
3L;Z6~38 Preparation A quantity of 2.5 g plperidine i3 added to a solution of 2.4 g 2-Eormyl-1,3-indanedione in 40 ml ethyl alcohol. The mixture is heated in a water bath for 20 minutes. It is subsequently filtered after cooling. The precipitate is recry~tallized in ethyl alcohol. The yield is 44~.
Physiochemical Properties Melting point: 167~C (ethyl alcohol).
NMR spectrum in CDC13: 7.77 ppm, multiplet, 4 protons, aromatic phthalyl hydride; 7.6 ppm, singlet, 1 proton, CH; 4.53 ppm, multiplet, 2 protons, CH2 at 2 or 6 on the piperidine nucleus; 3.67 ppm, multiplet, 2 protons, CH2 at 2 or 6 on the piperidine nucleus; 1.83 ppm, multiplet, 6 protons, CH2 at 3, 4 and S on the piperidine nucleus.
Example IX
2-Dimethylaminomethylene-1,3-indanedione. Pro~uct of formula (I) in which Rl - R2 = CH3; code name COR3761.
Pre~aration Five milliliters of a 25~ dimethylamine solution in ethyl alcohol is added to a solution of 2.7 g 2-formyl-1,3-indanedione in 60 ml ethyl aLcohol. The mixture is heated at approxi~ately 40C for four hours. The solvent i8 removed by evaporation. The precipitate i9 isolated, then recrystallized in a mixture o isopropyl ~ther/ethyl alcohol (8/2). The yiela is 58%.
PhysicochemicaL Properties Melting point: 138C (ethyl alcohol).
MNR spectrum in CDC13: 7.8 ppm, multiplet, 4 protons, aromatic p~thalyl hydride; 7.6 ppm, singlet, 1 proton, =CH; 3.93 ppm, singlet, 3 proton, CH3;
3.42 ppm, singlet, 3 protons, CH3.
Example X
l-Perhydroazepinyl-2-methylene-1,3-indanedione.
Product of formula (I) in w~ich NR1R2 = N(CH2)6; code name COR3790.
Preparation Three milliliters hexamethylenimine is added to a solution of 1.6 g 2-ormyl-1,3-indanedione in 40 ml ethyl aIcohol. The mixture is 'neated in a water bath form 60 minutes. The ethyl alcohol is partially evaporated. The residue i8 refrigerated for 12 hours. The precipitate is filtered and then purified by passing over a silica column using ethyl ether as the eluent. The yield is 43%.
Physicochemical Properties Melting point: 125C (ethyl alcohol).
IR spectrum: ~O bands at 1700 and 1650 cm-l NMR spectrum in CDC13: 7.78 pprn, multiplet, 4 protons, aromatic phthalyl ~ydride; 7.63 ppm, singlet, 1 proton, CH; 4.50 ppm, multiplet, 2 ~rotons, CH2 at 2 or 7 on the perhydroazepinyl nucleus; 3.67 ppm, multiple-t, 2 protons, CH2 at 3, 4, S and 6 on the perhydroazepinyl nucleus.
The results of the toxicological and pharmacological studies performed on the products according to the present invention are reported below.
Toxicity CoR3726, COR3754, COR3755, COR3756, CoR3757~
COR3758, COR3759, COR3751, and coR379o caused no deaths in mice in an oral dose of 300 mg/kg or an intraperitoneal dose of 200 mg/kg. When administered to mice orally, dissolved in 20% TWEEN*, COR3761 exhibited an LD50 of 520 (457-592~ mg/kg.
Pharmacolo~y Diuretic activity was determined in several experimental models. In rats subjected to excess water intake, CoR376 and COR3761, administered in an oral dose of 20 mg/kg, increased urinary sodium excretion by * Trademark , , ~6~
a factor of 4.4 and 3.5, respectively. Spironolactone adminis-tered under -the same conditions and in the same dose increased sodium excretion by 3.6. ~hen given orally to rats subjected to excess sodium chloride intake, COR3761 produced the following increments in volumetric urinary excretion measured at the sixth hour: 10~ in a dose oE 10 mg/kg, 42!.5% in a dose o~
20 mg/kg and 68.4% in a dose o~ 40 mg/kg. COR3761 was administered to rats subjected to excess water intake and volumetric urinary excretion and sodium and potassium elimination were measured over a period of six ~ours. These parameters were, respectively, -13%, +73~, +77% af-ter administration of 10 mg/kg; +9%, +241%, ~114~ after 20 mg/kg and -4%, +532~, +138% after 40 mg/kg. The sodium/potassium ratio which was 0.4 in the control animals was 0.47 at 10 mg/kg, 0.62 at 20 mg/kg and 1.48 at 40 mg/kg. In the course of another experiment, volumetric urniary excretion and sodium and potassium elimination were, respectively: +1%, +100%, +54% at 20 mg/kg; +10%, +313~, +69~ at 40 mg/kg and +16%, ~356~ and +89% at 60 mg/kg. The sodium/potassium ratio went from 0.43 in the control animals to 0.53 at 20 mg per kg, 1.02 at 40 mg/kg and 1.12 at j60 mg/kg.
Spasmolytic activity was determined in vitro by measurement of t~e e:Efect of the test product on ileum contractions in guinea pigs induced by transmural ~4~ 3~
-la-electric transmission in an oxygenated Krebs solution at 32aC. When used in a concentration of 0.5 mcg/ml, COR3754 and COR3759 in~ibited these contractions by 50%. Domperidone ex~ibits ~he same activity in a concentration of 1 mcg/ml~
Anti-inflammatory activity was determined in rats by measurement of in~ibition oE the edema induc~d by intraplantar injection oE 0.1 ml of a 1~ carragheenin suspension. The test products were administered orally one hour before the carragheenin injection and the determination was made three hours after injection.
Doses of 100 mg/kg COR3755 and COR3761 produced 3G% and 49~ in~ibition, respectively. Aspirin administered under the same conditions in a dose oE 150 mg/kg produced 40% inhibition o the ede~a.
Bronchodilating activity was determined in vitro by measuremsnt of the flow of Tyrode's solution through an isolated and perfused guinea pig lung which had been contracted by addition of 0.05 mcg/ml methacholine to the perfusion liquid. CoR3755, CoR3757, COR3759, COR3761, COR3762 and COR3790, which were used, respectively, in concentrations of 50, 100, 10, 10, 25 and 100 mcg/ml, increased the flow by 50~.
Amino~hylline produces t'nis same efEect in a concentration of 100 mcg/ml.
3~3 Anticholinergic activity was evaluated by measuremPnt of the cont~actions inauced by 0.1 mcg/ml acetylcholine ln isolated segments of guinea pig ileum. When used in concentrations of 100, 50, 10, 50, 10 and 25 mcg/ml, respectively, CoR3755~ COR3757, COR3761, COR3762 and C0~3790 produced an 80~ inhibition of these contractions.
Central anticholinergic activity was evaluated by measurement of inhibition, under the test product, of muscular tremors induced in mice by ~ubcutaneous injection of 0.5 mg/kg oxotremorine. The tremors are rated according to an index ranging from O to 6, one hour after intraperitoneal injection of the test product. An index of O indicates absence of tremor while 6 represents maximum tremor. COR3762 administered in a dose of 100 mg/kg resulted in an index of 3; imipramine, given under the same conditions in a dose of 25 mg/kg produced the same activity.
~ ntidepressant activity was determined in the test involving potentiation of yohimbine toxicity and in the test involving in~ibition of reserpine-induced ptosis.
One hour before oral administration of the test product, a non-lethal dose of yohimbine, i.e., 15 mg/kg-doses of COR3761 and COR3762 produced 80% and 100% mortality, respectively.
Mice were given an oral dose oE the test product ninety minute~s beEore intraperitoneal injection of 5 mg/kg dissolved reserpine. Ptosis was evaluated according to an index oE 0 to 6, ~here 0 signifies ptosis and ~ indicates absence of pto~is. Under the experimental conditions, COR3761 and COR3762 in doses of 200 and 50 mg/kg, respectively, produces respective ratings of 5 and 4.
In view oE their p~armacological activity, which is associated with low toxicity, the products of the present invention can be used in human or ve-terinary therapy.
~ len combined with -the conventional vehicles, they can e.g., be utilized in -the treatment of cardiac, renal or hepatic edema and arterial hypertension, in the -treatment of spasmodic symptoms, especially of the digestive and respiratory systems, in the treatment oE
asthma conditions or for depressive states.
When combined with the conventional vehicles, depending on the indication, they can be administered e.g., by the oral route in the form of dragees, tables, syrups, vials; rectally in the form of suppositories:
by -the intramuscular route or the intravenous route.
According to the indication and the subject, dodes administered range ~rom 1-100 mg/day given in one to six administrations orally, from 1-100 mg/day given in ~166~3~3 one or two admini~trations rectally and from 0.5-50 mg given by parenteral injection.
Obviously, numerous modificatiolls and variation~
of the present invention are possible in light to the above teaching.s. It is therefore to be understood that within the scope of the appended cla:ims, the inv~ntion may be practiced otherwise than as specifically described herein.
Claims (13)
1. A pharmaceutical composition, comprising:
(i) an effective amount of at least one product having the following structural formula (I) wherein R1 is a hydrogen atom or a C1-6 alkyl group; and R2 is a straight or branched C1-4 alkyl group, a cyclopropylmethyl group, a 2-furyl methyl group, a benzyl group, or a phenyl group; or NR1R2 is a nitrogenous heterocyclic compound N(CH2)n, where n is 4, 5 or 6, and (ii) a pharmaceutically or veterinarily acceptable excipient.
(i) an effective amount of at least one product having the following structural formula (I) wherein R1 is a hydrogen atom or a C1-6 alkyl group; and R2 is a straight or branched C1-4 alkyl group, a cyclopropylmethyl group, a 2-furyl methyl group, a benzyl group, or a phenyl group; or NR1R2 is a nitrogenous heterocyclic compound N(CH2)n, where n is 4, 5 or 6, and (ii) a pharmaceutically or veterinarily acceptable excipient.
2. The pharmaceutical composition of Claim 1, wherein R1 is methyl or ethyl.
3. The pharmaceutical composition of Claim 1, wherein R2 is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, or tertiary butyl.
4. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is methyl.
5. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is ethyl.
6. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is phenyl.
7. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is isobutyl.
8. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is isopropyl.
9. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is cyclopropylmethyl.
10. The pharmaceutical composition of Claim 1, wherein R1 is hydrogen and R2 is 2-furyl methyl.
11. The pharmaceutical composition of Claim 1, wherein NR1R2 is N(CH2)5.
12. The pharmaceutical composition of Claim 1, wherein R1 and R2 are both methyl.
13. The pharmaceutical composition of Claim 1, wherein NR1R2 is N(CH2)6.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8411678A FR2567754B1 (en) | 1984-07-20 | 1984-07-20 | THINAPEUTIC APPLICATION OF AMINOMETHYLENE-2 INDANEDIONES-1,3 SUBSTITUTED ON NITROGEN |
| FR84.11.678 | 1984-07-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1266438A true CA1266438A (en) | 1990-03-06 |
Family
ID=9306403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000486914A Expired - Fee Related CA1266438A (en) | 1984-07-20 | 1985-07-17 | Therapeutic application of n-substituted 2- aminomethylene-1,3-indanediones |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US4758561A (en) |
| EP (1) | EP0172128B1 (en) |
| JP (1) | JPS6144812A (en) |
| CA (1) | CA1266438A (en) |
| DE (1) | DE3571128D1 (en) |
| ES (1) | ES8604420A1 (en) |
| FR (1) | FR2567754B1 (en) |
| MA (1) | MA20491A1 (en) |
| OA (1) | OA08067A (en) |
| PT (1) | PT80830B (en) |
| ZA (1) | ZA855462B (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH06508375A (en) * | 1992-04-03 | 1994-09-22 | イノテラ | Derivatives of indan-1,3-dione and indan-1,2,3-trione, processes for their preparation and their therapeutic uses |
| US6231594B1 (en) * | 1999-08-11 | 2001-05-15 | Radiant Medical, Inc. | Method of controlling body temperature while reducing shivering |
| US6306403B1 (en) * | 2000-06-14 | 2001-10-23 | Allergan Sales, Inc. | Method for treating parkinson's disease with a botulinum toxin |
| US6582457B2 (en) | 2001-02-15 | 2003-06-24 | Radiant Medical, Inc. | Method of controlling body temperature while reducing shivering |
-
1984
- 1984-07-20 FR FR8411678A patent/FR2567754B1/en not_active Expired
-
1985
- 1985-06-19 EP EP85450015A patent/EP0172128B1/en not_active Expired
- 1985-06-19 DE DE8585450015T patent/DE3571128D1/en not_active Expired
- 1985-07-16 MA MA20716A patent/MA20491A1/en unknown
- 1985-07-17 CA CA000486914A patent/CA1266438A/en not_active Expired - Fee Related
- 1985-07-18 PT PT80830A patent/PT80830B/en not_active IP Right Cessation
- 1985-07-18 JP JP60159231A patent/JPS6144812A/en active Pending
- 1985-07-19 ZA ZA855462A patent/ZA855462B/en unknown
- 1985-07-19 ES ES545422A patent/ES8604420A1/en not_active Expired
- 1985-07-19 OA OA58646A patent/OA08067A/en unknown
- 1985-07-22 US US06/757,499 patent/US4758561A/en not_active Expired - Fee Related
-
1987
- 1987-01-21 US US07/005,657 patent/US4757067A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| OA08067A (en) | 1987-03-31 |
| FR2567754A1 (en) | 1986-01-24 |
| PT80830A (en) | 1985-08-01 |
| EP0172128A1 (en) | 1986-02-19 |
| PT80830B (en) | 1987-09-30 |
| JPS6144812A (en) | 1986-03-04 |
| FR2567754B1 (en) | 1987-05-29 |
| ES8604420A1 (en) | 1986-02-01 |
| US4758561A (en) | 1988-07-19 |
| DE3571128D1 (en) | 1989-07-27 |
| EP0172128B1 (en) | 1989-06-21 |
| ES545422A0 (en) | 1986-02-01 |
| US4757067A (en) | 1988-07-12 |
| ZA855462B (en) | 1986-03-26 |
| MA20491A1 (en) | 1986-04-01 |
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