DE20204129U1 - Agent for coloring keratin fibers with quinolinium dyes - Google Patents
Agent for coloring keratin fibers with quinolinium dyesInfo
- Publication number
- DE20204129U1 DE20204129U1 DE20204129U DE20204129U DE20204129U1 DE 20204129 U1 DE20204129 U1 DE 20204129U1 DE 20204129 U DE20204129 U DE 20204129U DE 20204129 U DE20204129 U DE 20204129U DE 20204129 U1 DE20204129 U1 DE 20204129U1
- Authority
- DE
- Germany
- Prior art keywords
- ethyl
- group
- quinolinium salts
- quinolinium
- salts
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/35—Ketones, e.g. benzophenone
- A61K8/355—Quinones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
Description
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßt The description text was not recorded electronically
Der Beschreibungstext wurde nicht elektronisch erfaßtThe description text was not recorded electronically
Claims (12)
wobei in der Formel (I) die Restgruppen R1 bis R7, W und A- die folgende Bedeutung haben:
R1 ist gleich einer geradkettigen oder verzweigten (C1-C8)-Alkylgruppe, einer geradkettigen oder verzweigten (C1-C8)-Alkoxy-(C1-C8-alkylgruppe;
R2, R3, R4, R5, R6 und R7 sind unabhängig voneinander gleich einem Wasserstoffatom, einer geradkettigen oder verzweigten (C1-C4)-Alkylgruppe oder einer geradkettigen oder verzweigten (C1-C4)-Hydroxyalkylgruppe, einer Hydroxygruppe, einer Methoxygruppe, einer Benzylgruppe, einer Arylgruppe, einer Heteroarylgruppe, einem Halogenatom, einer Nitrogruppe, einer Nitrosogruppe, einer Cyanogruppe, einer Trifluormethyl gruppe, einer -CO2Ra-Gruppe, einer -CONHRa-Gruppe, einer CON(Ra)2- Gruppe, einer -O(CO)Ra-Gruppe, einer -OCH2Aryl-Gruppe, einer -SO2NH2-Gruppe, einer -NH2-Gruppe, einer -NHRa-Gruppe, einer -N(Ra)2- Gruppe, einer -NHCORa-Gruppe, einer -NHCOORa-Gruppe, einer -CH2NHRa-Gruppe, einer -CH2N(Ra)2-Gruppe, einer -PO(ORa)2-Gruppe, einer -SO2CHF2-Gruppe, einer -SO2CF3-Gruppe, einer -SO2Ra-Gruppe oder einer -SRa-Gruppe, wobei Ra gleich einem Wasserstoffatom, einem gegebenenfalls substituierten aromatischen Carbozyklus oder Heterozyklus, einem gegebenenfalls substituierten nichtaromatischen Carbozyklus oder Heterozyklus oder einer (C1-C6)-Alkylgruppe ist, mit der Massgabe, dass zwei nebeneinanderliegende Reste R1 bis R7 auch gemeinsam mit den Kohlenstoffatomen des aromatischen Kerns einen 5- oder 6gliedrigen nichtaromatischen oder aromatischen Ring bilden können, der gegenenenfalls ein oder mehrere Schwefelatome, Stickstoffatome und/oder Sauerstoffatome enthalten kann;
W ist gleich einem Rest der nachfolgenden Formeln (W1) bis (W4)
wobei gilt:
Q1, Q2 und Q3 sind unabhängig voneinander gleich einem Wasserstoffatom, einem gegebenenfalls substituierten einkernigen oder mehrkernigen anellierten aromatischen Carbozyklus oder Heterozyklus, einer geradkettigen oder verzweigten (C1-C6)-Alkylgruppe, einer geradkettigen oder verzweigten (C1-C4)-Hydroxyalkylgruppe, einer geradkettigen oder verzweigten (C1-C4)-Aminoalkylgruppe, einer geradkettigen oder verzweigten (C1-C4)-Alkylthioethergruppe, einer Di(C1-C4)-alkylaminogruppe, einer Di(C1-C4-hydroxyalkyl)aminogruppe, einer (C1-C4)-Hydroxyalkylaminogruppe, einer (C1-C4)-Alkoxygruppe, einer Benzylgruppe, einer -CORb-Gruppe, oder einer -CO2Rb-Gruppe, wobei Rb gleich einem Wasserstoffatom, einem gegebenenfalls substituierten aromatischen Carbozyklus oder Heterozyklus, einem gegebenenfalls substituierten nichtaromatischen Carbozyklus oder Heterozyklus, einer geradkettigen oder verzweigten (C1-C6)-Alkylgruppe, einer geradkettigen oder verzweigten (C1-C4)-Hydroxyalkylgruppe oder einer geradkettigen oder verzweigten (C1-C4)-Aminoalkylgruppe ist; und
A- ist gleich dem Anion einer organischen oder anorganischen Säure.1. Agent for coloring keratin fibers, characterized in that it contains at least one compound of the formula (I):
where in the formula (I) the residual groups R1 to R7, W and A - have the following meaning:
R1 is equal to a straight-chain or branched (C 1 -C 8 ) alkyl group, a straight-chain or branched (C 1 -C 8 ) alkoxy (C 1 -C 8 alkyl group;
R2, R3, R4, R5, R6 and R7 are independently a hydrogen atom, a straight or branched (C 1 -C 4 ) alkyl group or a straight or branched (C 1 -C 4 ) hydroxyalkyl group, a hydroxy group, one Methoxy group, a benzyl group, an aryl group, a heteroaryl group, a halogen atom, a nitro group, a nitroso group, a cyano group, a trifluoromethyl group, a -CO 2 R a group, a -CONHR a group, a CON (R a ) 2 - Group, an -O (CO) R a group, an -OCH 2 aryl group, an -SO 2 NH 2 group, an -NH 2 group, an -NHR a group, an -N (R a ) 2 group, an -NHCOR a group, an -NHCOOR a group, a -CH 2 NHR a group, a -CH 2 N (R a ) 2 group, a -PO (OR a ) 2 Group, an -SO 2 CHF 2 group, an -SO 2 CF 3 group, an -SO 2 R a group or an -SR a group, where R a is a hydrogen atom, an optionally substituted aromatic carbocycle or H is heterocycle, an optionally substituted non-aromatic carbocycle or heterocycle or a (C 1 -C 6 ) alkyl group, with the proviso that two adjacent radicals R1 to R7 together with the carbon atoms of the aromatic nucleus also form a 5- or 6-membered non-aromatic or aromatic ring can form, which can optionally contain one or more sulfur atoms, nitrogen atoms and / or oxygen atoms;
W is equal to a remainder of the following formulas (W1) to (W4)
where:
Q1, Q2 and Q3 independently of one another are equal to a hydrogen atom, an optionally substituted mononuclear or polynuclear fused aromatic carbocycle or heterocycle, a straight-chain or branched (C 1 -C 6 ) alkyl group, a straight-chain or branched (C 1 -C 4 ) - Hydroxyalkyl group, a straight-chain or branched (C 1 -C 4 ) aminoalkyl group, a straight-chain or branched (C 1 -C 4 ) alkylthioether group, a di (C 1 -C 4 ) alkylamino group, a di (C 1 -C 4 -hydroxyalkyl) amino group, a (C 1 -C 4 ) hydroxyalkylamino group, a (C 1 -C 4 ) alkoxy group, a benzyl group, a -COR b group, or a -CO 2 R b group, where R b is a hydrogen atom, an optionally substituted aromatic carbocycle or heterocycle, an optionally substituted non-aromatic carbocycle or heterocycle, a straight-chain or branched (C 1 -C 6 ) alkyl group, a straight-chain or branched (C 1 -C 4 ) hydroxyalkyl group or a straight-chain or branched (C 1 -C 4 ) aminoalkyl group; and
A - is equal to the anion of an organic or inorganic acid.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE20204129U DE20204129U1 (en) | 2002-03-15 | 2002-03-15 | Agent for coloring keratin fibers with quinolinium dyes |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE20204129U DE20204129U1 (en) | 2002-03-15 | 2002-03-15 | Agent for coloring keratin fibers with quinolinium dyes |
Publications (1)
Publication Number | Publication Date |
---|---|
DE20204129U1 true DE20204129U1 (en) | 2002-07-25 |
Family
ID=7968980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE20204129U Expired - Lifetime DE20204129U1 (en) | 2002-03-15 | 2002-03-15 | Agent for coloring keratin fibers with quinolinium dyes |
Country Status (1)
Country | Link |
---|---|
DE (1) | DE20204129U1 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1568694A1 (en) * | 2004-02-27 | 2005-08-31 | L'oreal | N-heteroaryl-para-phenylene diamines for colouring hair |
US7329288B2 (en) | 2004-02-27 | 2008-02-12 | L'oreal S.A. | N-heteroaryl secondary para-phenylenediamine, a dye composition comprising such a para-phenylenediamine, a process for preparing this composition and use thereof |
US7989462B2 (en) | 2003-07-03 | 2011-08-02 | Myrexis, Inc. | 4-arylamin-or-4-heteroarylamino-quinazolines and analogs as activators of caspases and inducers of apoptosis and the use thereof |
US8258145B2 (en) | 2005-01-03 | 2012-09-04 | Myrexis, Inc. | Method of treating brain cancer |
US8309562B2 (en) | 2003-07-03 | 2012-11-13 | Myrexis, Inc. | Compounds and therapeutical use thereof |
US10479797B2 (en) | 2016-06-06 | 2019-11-19 | Arena Pharmaceuticals, Inc. | Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto |
-
2002
- 2002-03-15 DE DE20204129U patent/DE20204129U1/en not_active Expired - Lifetime
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7989462B2 (en) | 2003-07-03 | 2011-08-02 | Myrexis, Inc. | 4-arylamin-or-4-heteroarylamino-quinazolines and analogs as activators of caspases and inducers of apoptosis and the use thereof |
US8309562B2 (en) | 2003-07-03 | 2012-11-13 | Myrexis, Inc. | Compounds and therapeutical use thereof |
EP1568694A1 (en) * | 2004-02-27 | 2005-08-31 | L'oreal | N-heteroaryl-para-phenylene diamines for colouring hair |
FR2866887A1 (en) * | 2004-02-27 | 2005-09-02 | Oreal | N-HETEROARYL SECONDARY PARA-PHENYLENEDIAMINE, TINCTORIAL COMPOSITION COMPRISING SUCH A PARA-PHENYLENEDIAMINE, PROCESS USING THE SAME AND USE THEREOF |
US7329288B2 (en) | 2004-02-27 | 2008-02-12 | L'oreal S.A. | N-heteroaryl secondary para-phenylenediamine, a dye composition comprising such a para-phenylenediamine, a process for preparing this composition and use thereof |
US8258145B2 (en) | 2005-01-03 | 2012-09-04 | Myrexis, Inc. | Method of treating brain cancer |
US10479797B2 (en) | 2016-06-06 | 2019-11-19 | Arena Pharmaceuticals, Inc. | Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto |
US10662200B2 (en) | 2016-06-06 | 2020-05-26 | Arena Pharmaceuticals, Inc. | Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto |
US10927123B2 (en) | 2016-06-06 | 2021-02-23 | Arena Pharmaceuticals, Inc. | Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto |
US11560386B2 (en) | 2016-06-06 | 2023-01-24 | Arena Pharmaceuticals, Inc. | Modulators of the beta-3 adrenergic receptor useful for the treatment or prevention of disorders related thereto |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1997340B (en) | Disulfide dyes, composition comprising them and method of dyeing | |
US4329504A (en) | Metaphenylenediamines | |
CN103442682B (en) | Comprise 1-hexyl/heptyl-4,5-diamino-pyrazole and naphthalene-1-phenol and the oxidative dye compositions of derivant thereof | |
CA2277893A1 (en) | 4-(3-heterocyclyl-1-benzoyl)pyrazoles and their use as herbicides | |
CN101010062A (en) | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof | |
DE20204129U1 (en) | Agent for coloring keratin fibers with quinolinium dyes | |
CN104114540A (en) | 1-hexyl-1h-pyrazole-4,5-diamine hemisulfate, and its use in dyeing compositions | |
DE69414314T3 (en) | Keratinic fiber oxidation dye containing a para-aminophenol, a meta-aminophenol and a metaphenylene diamine | |
CN102046606A (en) | Keratin dyeing compounds, keratin dyeing compositions containing said compounds, and use thereof | |
CN102015646B (en) | Azomethine direct dyes or reduced precursors of these dyes obtained from 2-amino-3-hydroxypyridine, and hair dyeing process using these dyes and precursors | |
DE2364114B2 (en) | o-Nitrodiphenylamine dyes and preparations for coloring hair containing a nitrodiphenylamine as a dye | |
WO2001010379A3 (en) | Dyeing agent for keratinous fibres | |
JPS5967216A (en) | Hair dye | |
MX2008014473A (en) | Disazo acid dyes. | |
CN110087628A (en) | Method for using at least one specific triarylmethane dye and at least one fluorescent dyeing keratin fiber | |
EP0391264A1 (en) | Reactive dyes with two or three halogen-N-heterocycles as reactive groups | |
US3909190A (en) | Hair dyeing process and composition containing {60 -cyano-methanesulfonamido-nitrobenzene derivatives | |
CN101010118A (en) | Keratin dyeing compounds, keratin dyeing compositions containing them, and use thereof | |
AU2005297546A1 (en) | Cationic azacyanine dyes and colorants containing these | |
CN110099671A (en) | Use the method for at least one specific azine dye and at least one fluorescent dyeing keratin fiber | |
JPS63162615A (en) | Oxidative dyestuff | |
US3907494A (en) | Hair dyes based on diamino-nitro-benzene compounds | |
WO2014202150A1 (en) | New cationic dyes, kits and compositions thereof, and process for dyeing keratin fibers | |
DE19825202A1 (en) | Tris and polyazo dyes and their mixtures | |
DE69930095T2 (en) | Use of cationic monobenzene anilines for dyeing keratin fibers, compositions and dyeing methods |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
R207 | Utility model specification |
Effective date: 20020829 |
|
R150 | Term of protection extended to 6 years |
Effective date: 20050411 |
|
R079 | Amendment of ipc main class |
Free format text: PREVIOUS MAIN CLASS: A61K0007130000 Ipc: A61K0008490000 |
|
R151 | Term of protection extended to 8 years |
Effective date: 20080220 |
|
R152 | Term of protection extended to 10 years |
Effective date: 20100301 |
|
R081 | Change of applicant/patentee |
Owner name: WELLA GMBH, DE Free format text: FORMER OWNER: WELLA AG, 64295 DARMSTADT, DE Effective date: 20110720 |
|
R071 | Expiry of right | ||
R071 | Expiry of right |