EP1372585A1

EP1372585A1 - Oxidation dyeing composition 3-amino pyrazolo- 1,5-a]-pyridine and one pyrazolotriazole coupling agent

Info

Publication number: EP1372585A1
Application number: EP02753738A
Authority: EP
Inventors: Sylvain Kravtchenko; Alain Lagrange
Original assignee: LOreal SA
Current assignee: LOreal SA
Priority date: 2001-03-27
Filing date: 2002-03-27
Publication date: 2004-01-02
Also published as: WO2002076418A1; FR2822691B1; FR2822691A1

Abstract

The invention relates to novel compositions for the oxidation dyeing of keratin fibres comprising at least one 3-amino pyrazolo-[1,5-a]-pyridine as oxidation base and at least one particular pyridine coupling agent. The invention also relates to a dyeing method and a device using said composition.

Description

COMPOSITION FOR OXIDATION DYE 3-AMINO PYRAZOLO- * 1. 5-AL-PYRIDINE AND A PYRAZOLOTRIAZOLE COUPLER

The subject of the invention is new compositions for the oxidation dyeing of keratin fibers comprising at least one 3-amino pyrazolo- [1, 5-a] - pyridine as oxidation base and at least one particular pyridine coupler. , a dyeing process as well as a dyeing device using this composition.

It is known to dye keratin fibers and in particular human hair with dye compositions containing oxidation dye precursors, in particular ortho or paraphenylenediamines, ortho or paraaminophenols, heterocyclic compounds such as diaminopyrazole derivatives, called generally oxidation bases. The precursors of oxidation dyes, called oxidation bases, are colorless or weakly colored compounds which, associated with oxidizing products, can give rise, through an oxidative condensation process, to colored and coloring compounds. These compounds have in common that they have an amino group and a hydroxyl group or two amino groups, which gives them their basic oxidation character. It is also known that the shades obtained with these oxidation bases can be varied by combining them with couplers or color modifiers, the latter being chosen in particular from aromatic metadiamines, metaaminophenols, metadiphenols and certain heterocyclic compounds.

The variety of molecules involved in the oxidation bases and couplers, allows obtaining a rich palette of colors.

The so-called "permanent" coloration obtained thanks to these oxidation dyes must moreover satisfy a certain number of requirements. Thus, it must be without drawbacks from the toxicological point of view, it must make it possible to obtain nuances in the desired intensity, to have good resistance to external agents (light, bad weather, washing, permanent waving, perspiration, friction).

The dyes must also make it possible to cover white hair, and finally be the least selective possible, that is to say allow to obtain the smallest possible color differences throughout the same keratin fiber, which can be in differently sensitized effect (ie damaged) between its tip and its root. Pyridines are already known for the oxidation dyeing of keratin fibers as oxidation bases. For example, GB 1,026,978 and

GB 1,153,196 suggest using 2,5-diamino pyridine, 2- (4-methoxyphenyl) amino

3-amino pyridine, 2,3-diamino 6-methoxy pyridine, 2- (β-methoxyethyl) εmino 3- amino 6-methoxy pyridine, 3,4-diamino pyridine as the oxidation base.

In addition, it is known to use certain couplers of the pyridine type for the oxidation dyeing of keratinous fibers, for example in patent applications DE 3132885, DE 3233540, and DE 1149496.

The object of the invention is to develop new dye compositions which make it possible to obtain a new range of colors and which do not have the drawbacks of dyes of the prior art. In particular, the invention aims to develop compositions which lead to very powerful colorings, particularly resistant to the various aggressions which the hair can undergo (light, bad weather, washing, permanent waving, perspiration, friction), not very selective and having good safety.

To this end, the subject of the invention is a composition for the oxidation dyeing of keratin fibers, comprising in a medium suitable for dyeing,

As an oxidation base at least one 3-amino pyrazolo- [1,5-a] - pyridine of the following formula (I) and / or one of its addition salts with an acid or with a base:

in which :

- R _{1 s} R ₂ , R ₃ , R and R ₅ , identical or different, represent a hydrogen or halogen atom; a radical -NHS0 ₃ H; a hydroxyl radical; an alkyl radical; an alkoxy radical; an alkylthio radical; an amino radical; a monoalkylamino radical; a dialkylamino radical in which the two alkyl groups can, together with the nitrogen atom to which they are bonded, form a ring can be interrupted by one or more nitrogen, oxygen or sulfur atoms; a heterocycle; a nitro radical; an aryl radical; a C1-C4 acyl radical; an alkoxy (CrC) carbonyl radical; a carboxamido radical; a cyano radical; a radical - CO ₂ H, a radical -SO ₃ H; a radical -PO ₃ H ₂ ; a radical -P0 ₄ H ₂ ; or a group of the following formula (II):

in which X and R represent, independently of each other, an oxygen atom, an NH or N (CC) alkyl group, and Y represents a hydroxyl, amino, alkyl, alkoxy, alkylamino, or dialkylamino radical, and

• at least one diamino or triamino pyridine coupler of formulas (III), (IV) or (V) below:

in which - R7 and R10, identical or different, represent a hydrogen atom; an alkyl radical,

- R8 and R9, identical or different, represent a hydrogen atom, an alkyl radical, an alkoxy radical, an amino radical, a nitrile radical, an alkylamino radical, a dialkylamino radical, a carboxyl radical, an alkoxycarbonyl radical, a radical amido, an amidoalkyl radical, a halogen atom, an alkylthio radical, it being understood that at most one of the groups R8 and R9 denotes an amino, alkylamino or dialkylamino radical.

In the compounds of formula (I), (III), (IV) or (V) useful for the present invention, the term alkyl used for the alkyl radicals as well as for the groups comprising an alkyl part means, unless otherwise indicated, a carbon chain, linear or branched, comprising from 1 to 30 carbon atoms which can be interrupted by one or more oxygen, sulfur or nitrogen atoms, and which can be substituted by one or more groups chosen from halogen atoms such as chlorine, bromine, iodine and fluorine; heterocycles; the radicals aryl, hydroxyl, alkoxyl, amino, acyl, carboxamido, -CO ₂ H, -SO ₃ H, -PO ₃ H ₂ , -PO ₄ H ₂ , -NHS0 ₃ H, sulfonamide, monoalkylamino, trialkylammonium, or even by a dialkylamino radical in which the two alkyl groups can form, together with the nitrogen atom of said dialkyl (CτC ₄ ) amino group to which they are linked, a cycle which can be interrupted by one or more nitrogen, oxygen or sulfur.

Similarly, according to the invention, in formulas (I), (III), (IV) or (V), the term alkoxy used for the alkoxy radicals as well as for the groups comprising an alkoxy part, means, unless otherwise indicated, an O-alkyl chain, the term alkyl having the meaning indicated above.

According to the invention, for formula (I), the term “heterocycle” means an aromatic or non-aromatic cycle containing 5, 6 or 7 vertices, and from 1 to 3 heteroatoms chosen from nitrogen, sulfur and oxygen atoms . These heterocycles can be condensed on other heterocycles or on a phenyl group. They can be substituted by a halogen atom; an alkyl radical; an alkoxy radical; a hydroxyl radical; an amino radical; an alkylamino radical; dialkylamino in which the two alkyl groups can, together with the nitrogen atom to which they are linked, form a ring which can be interrupted by one or more nitrogen, oxygen or sulfur atoms. These heterocycles can, moreover, be quaternized by an alkyl radical. The terms alkyl and alkoxy have the meanings indicated above.

Among these heterocycles, mention may in particular be made, by way of example, of the cycles: thiadiazole, triazole, isoxazole, oxazole, azaphosphole, thiazole, isothiazole, imidazole, pyrazole, triazine, thiazine, pyrazine, pyridazine, pyrimidine, pyridine, diazepine, oxazepine, benzotriazole, benzoxazole, benzimidazole, benzothiazole, morpholine, piperidine, piperazine, azetidine, pyrrolidine, aziridine, 3- (2- hydroxyethyl) benzothiazol-3-ium, and 1- (2-hydroxyethyl) -pyridinium.

According to the invention, for formula (I), the term “aryl” is intended to mean an aryl radical which may be substituted by one or more alkyl, alkoxy, acyl, cyano, carboxamido, -C0 ₂ H, -SO ₃ H, -P0 radicals ₃ H ₂ , -PO H ₂ , hydroxyl, amino, monoalkyl (CC ₄ ) amino, or dialkyl (CC ₄ ) amino in which the two alkyl groups can form, together with the nitrogen atom of said dialkyl group (CC) amino to which they are linked, a cycle which can be interrupted by one or more nitrogen, oxygen or sulfur atoms. Preferably, the aryl group is a phenyl group which can be substituted as indicated above. Mention may in particular be made, among the groups of formula (II) above, of the acetamide, dimethylurea, O-methylcarbamate, methylcarbonate, N-dimethylcarbamate and esters groups.

The composition according to the invention preferably comprises the 3-amino pyrazolo- [1, 5-a] -pyridines corresponding to the following formula (la), as well as their addition salts with an acid or with a base:

in which :

Ri. ₂ , R ₃ , identical or different, represent a hydrogen or halogen atom; a radical -NHSO ₃ H; a hydroxyl radical; an alkyl radical; an alkoxy radical; an alkylthio radical; an amino radical; a monoalkylamino radical; a dialkylamino radical in which the two alkyl groups can form together with the nitrogen atom to which they are linked, a cycle which can be interrupted by one or more nitrogen, oxygen or sulfur atoms; a heterocycle; an acyl radical; an alkoxycarbonyl radical; a carboxamido radical; or a group of the following formula (II)

in which X and R represent, independently of one another, an oxygen atom, an NH or N (CrC ₄ ) alkyl group, and Y represents a hydroxyl, amino, alkyl, alkoxy, alkylamino or dialkylamino radical .

Among the 3-amino pyrazolo- [1, 5-a] -pyridines of formula (I), useful as oxidation base in the dye compositions of the invention, there may be mentioned in particular:

- pyrazolo [1,5-a] pyridin-3-ylamine;

- 2-acetylamino pyrazolo- [1,5-a] pyridin-3-ylamine;

- 2-morpholin-4-yl-pyrazolo [1, 5-a] pyridin-3-ylamine; - 3-amino-pyrazolo [1,5-a] pyridin-2-carboxylic acid;

- 2-methoxy-pyrazolo [1,5-a] pyridine-3-ylamino;

- (3-amino-pyrazolo [1,5-a] pyridine-7-yl) -methanol;

- 2- (3-amino-pyrazolo [1,5-a] pyridine-5-yl) -ethanol; - 2- (3-amino-pyrazolo [1,5-a] pyridine-7-yl) -ethanol;

- (3-amino-pyrazolo [1,5-a] pyridine-2-yl) -methanol;

- 3,6-diamino-pyrazolo [1,5-a] pyridine;

- 3,4-diamino-pyrazolo [1,5-a] pyridine;

- pyrazolo [1,5-a] pyridine-3,7-diamine; - 7-morpholin-4-yl-pyrazolo [1, 5-a] pyridin-3-ylamine;

- pyrazolo [1,5-a] pyridine-3,5-diamine;

- 5-morpholin-4-yl-pyrazolo [1, 5-a] pyridin-3-ylamine;

- 2 - [(3-amino-pyrazolo [1,5-a] pyridin-5-yl) - (2-hydroxyethyl) -amino] -ethanol;

- 2 - [(3-amino-pyrazolo [1,5-a] pyridin-7-yl) - (2-hydroxyethyl) -amino] -ethanol; - 3-amino-pyrazolo [1,5-a] pyridine-5-ol;

- 3-amino-pyrazolo [1,5-a] pyridine-4-ol;

- 3-amino-pyrazolo [1,5-a] pyridine-6-ol;

- 3-amino-pyrazolo [1,5-a] pyridine-7-ol; as well as their addition salts with an acid or with a base. The 3-amino pyrazolo- [1,5-a] -pyridines of formula (I) are known compounds, in particular in the pharmaceutical field, and are described in particular in US patent 5,457,200. These compounds can be prepared according to synthesis methods well known in the literature and as described for example in US patent 5,457,200. The 3-amino pyrazolo- [1, 5-a] -pyridines or formula (I) above and / or the addition salt (s) with an acid or a base preferably represent from 0.0001 to 10 % by weight approximately of the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately of this weight.

According to the invention, the pyridine coupler can be chosen from the following compounds

The couplers of formulas (III), (IV) or (V) are known in the art and can be prepared according to conventional syntheses.

According to a preferred embodiment, these couplers of formula (III), (IV) or (V) are chosen from 2,6-dimethoxy-3,5-diaminopyridine; 6-methoxy-N2-methyl-2,3-diaminopyridine; 6-methoxy-2,3-diaminopyridine; 2,6-diamino-pyridine.

The pyridine coupler (s) are preferably present in the composition in an amount between 0.0001 to 10% by weight approximately of the total weight

10 of the dye composition and even more preferably from 0.005 to 6% by weight approximately of this weight.

The medium suitable for dyeing, also called dye support, generally consists of water or a mixture of water and at least one organic solvent to dissolve the compounds which are not sufficiently soluble. in water. As organic solvent, mention may, for example, be made of lower C1-C4 alkanols, such as ethanol and isopropanol, polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, monoethyl ether and monomethyl ether of diethylene glycol, as well as aromatic alcohols such as benzyl alcohol or phenoxyethanol, analogues and their mixtures.

The solvents may be present in proportions preferably of between 1 and 40% by weight approximately relative to the total weight of the dye composition, and even more preferably between 5 and 30% by weight approximately.

The pH of the dye composition according to the invention is generally between 3 and 12 approximately, and preferably between 5 and 11 approximately. It can be adjusted to the desired value by means of acidifying or basifying agents usually used in dyeing keratinous fibers or even using conventional buffer systems.

Among the acidifying agents, there may be mentioned, by way of example, mineral or organic acids such as hydrochloric acid, orthophosphoric acid, sulfuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid, lactic acid, sulfonic acids. Among the basifying agents, there may be mentioned, by way of example, ammonia, alkali carbonates, alkanolamines such as mono-, di- and triethanolamines as well as their derivatives, sodium or potassium hydroxides and compounds of formula (III) below:

. in which W is a propylene residue optionally substituted by a hydroxyl group or a CC alkyl radical; R ₆ , R, R ₃ and R ₉ , identical or different, represent a hydrogen atom, an alkyl radical in CC ₄ or hydroxyalkyl in C-ι-C ₄ .

The composition according to the invention may contain, in addition to the pydidinic coupler of formula (III), additional couplers conventionally used for dyeing keratin fibers. Among these couplers, there may be mentioned in particular metaphenylenediamines, meta-aminophenols, metadiphenols, naphthalene couplers and heterocyclic couplers.

By way of example, mention may be made of 2-methyl 5-aminophenol, 5-N- (β-hydroxyethyl) amino 2-methyl phenol, 6-chloro-2-methyl-5-aminophenol, 3-amino phenol, 1,3-dihydroxy benzene, 1,3-dihydroxy 2-methyl benzene, 4-chloro 1,3-dihydroxy benzene, 2,4-diamino l- (β-hydroxyethyloxy) benzene, 2- amino 4- (β- hydroxyethylamino) 1-methoxybenzene, 1, 3-diamino benzene, 1, 3-bis- (2,4- diaminophenoxy) propane, 3-ureido aniline, 3-ureido 1-dimethylamino benzene , sesamol, 1-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2 methyl-1-naphtol, 6-hydroxy indole, 4-hydroxy indole, 4-hydroxy N-methyl indole, 6-hydroxy benzomorpholine, 2-amino-3-hydroxy pyridine, 1-N- (β- hydroxyethyl) amino-3,4-methylene dioxybenzene, 2,6-bis- (β- hydroxyethylamino) toluene and their addition salts.

When they are present, the additional coupler (s) preferably represent from 0.0001 to 10% by weight approximately of the total weight of the dye composition and even more preferably from 0.005 to 6% by weight approximately of this weight.

The dye composition according to the invention can also contain at least one additional oxidation base, and which can be chosen from the oxidation bases conventionally used in oxidation dyeing and among which mention may be made of paraphenylenediamines, bis -phenylalkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases other than the 3-amino pyrazolo- [1, 5-a] -pyridines of formula (I) used in accordance with the invention.

Among the paraphenylenediamines, mention may more particularly be made, for example, of paraphenylenediamine, paratoluylenediamine, 2-chloro paraphenylenediamine, 2,3-dimethyl paraphenylenediamine, 2,6-dimethyl paraphenylenediamine, 2,6-diethyl paraphenylenediamine , 2,5-dimethyl paraphenylenediamine, N, N-dimethyl paraphenylenediamine, N, N-diethyl paraphenylenediamine, N, N-dipropyl paraphenylenediamine, 4-amino N, N-diethyl 3-methyl aniline, N, N-bis- (β-hydroxyethyl) paraphenylenediamine, 4-N, N-bis- (β- hydroxyethyl) amino 2-methyl aniline, 4-N, N-bis- (β-hydroxyethyl) amino 2-chloro aniline , 2-β-hydroxyethyl paraphenylenediamine, 2-fluoro paraphenylenediamine, 2-isopropyl paraphenylenediamine, N- (β-hydroxypropyl) paraphenylenediamine, 2-hydroxymethyl paraphenylenediamine, N, N-dimethyl 3-methyl paraphenylenediamine, N, N- (ethyl, β-hydroxyethyl) paraphenylenediamine, N- (β, γ- dihydroxypropyl) paraphenylenediamine, N- (4'-aminophenyl) paraphenylenediamine, N-phenyl paraphenylenediamine, 2-phenyl hydroxyethyloxy paraphenylenediamine, 2- β-acetylaminoethyloxy paraphenylenediamine, N- (β-methoxyethyl) paraphenylenediamine, 4 aminophenyl pyrrolidine, 2-thienyl paraphenylene diamine, 2-β-hydroxy ethylamino-5-aminotol with an acid.

Among the para-phenylenediamines mentioned above, very particularly preferred are paraphenylenediamine, paratoluylenediamine, 2-isopropyl paraphenylenediamine, 2-β-hydroxyethyl paraphenylenediamine, 2-β-hydroxyethyloxy paraphenylenediamine, 2,6-dimethyl , 6-diethyl paraphenylenediamine, 2,3-dimethyl paraphenylenediamine, N, N-bis- (β-hydroxyethyl) paraphenylenediamine, 2-chloro paraphenylenediamine, 2-β-acetylaminoethyloxy paraphenylenediamine, and their addition salts with a acid. Mention may more particularly be made, among bis-phenylalkylenediamines, by way of example, of N, N'-bis- (β-hydroxyethyl) N, N'-bis- (4'-aminophenyl) 1, 3-diamino propanol, N, N'-bis- (β-hydroxyethyl) N, N'-bis- (4'-aminophenyl) ethylenediamine, N, N'-bis- (4-aminophenyl) tetramethylenediamine, N, N'-bis - (β-hydroxyethyl) N, N'-bis- (4-aminophenyl) tetramethylenediamine, N, N'-bis- (4-methyl-aminophenyl) tetramethylenediamine, N, N'-bis- (ethyl) N, N'-bis- (4'-amino, 3'-methylphenyl) ethylenediamine, 1, 8-bis- (2,5-diamino phenoxy) -3,5-dioxaoctane, and their addition salts with an acid.

Among the para-aminophenols, mention may more particularly be made, for example, of para-aminophenol, 4-amino 3-methyl phenol, 4-amino 3-fluoro phenol, 4-amino 3-hydroxymethyl phenol, 4-amino 2-methyl phenol, 4-amino 2-hydroxymethyl phenol, 4-amino 2-methoxymethyl phenol, 4-amino 2-aminomethyl phenol, 4-amino 2- (β-hydroxyethyl aminomethyl) phenol, 4-amino 2-fluoro phenol, and their addition salts with an acid.

Among the ortho-aminophenols, there may be mentioned more particularly by way of example, 2-amino phenol, 2-amino 5-methyl phenol, 2-amino 6-methyl phenol, 5-acetamido 2-amino phenol, and their addition salts with an acid.

Mention may more particularly be made, among heterocyclic bases, by way of example, of pyridine derivatives other than the compounds of formula (I) in accordance with the invention, pyrimidine derivatives and pyrazole derivatives. Among the pyridine derivatives other than the compounds of formula (I) in accordance with the invention, mention may be made more particularly of the compounds described for example in patents GB 1,026,978 and GB 1,153,196, such as 2,5-diamino pyridine, 2- (4-methoxyphenyl) amino 3-amino pyridine, 2,3-diamino 6-methoxy pyridine, 2- (β-methoxyethyl) amino 3-amino 6-methoxy pyridine, 3,4-diamino pyridine, and their addition salts with an acid.

Among the pyrimidine derivatives, mention may be made more particularly of the compounds described, for example, in patents DE 2,359,399; JP 88-169,571; JP 05 163 124; EP 0 770 375 or patent application WO 96/15765 such as 2,4,5,6-tetra-aminopyrimidine, 4-hydroxy 2,5,6-triaminopyrimidine, 2-hydroxy 4,5,6-triaminopyrimidine, 2,4-dihydroxy 5,6-diaminopyrimidine, 2,5,6-triaminopyrimidine, and pyrazolo-pyrimidine derivatives such as those mentioned in patent application FR-A-2 750 048 and among which may be mentioned pyrazolo - [1,5-a] -pyrimidine-3,7-diamine; 2,5-dimethyl pyrazolo- [1,5-a] -pyrimidine-3,7-diamine; pyrazolo- [1,5-a] - pyrimidine-3,5-diamine; 2,7-dimethyl pyrazolo- [1,5-a] -pyrimidine-3,5-diamine; 3-amino pyrazolo- [1,5-a] -pyrimidin-7-ol; 3-amino pyrazolo- [1,5-a] -pyrimidin-5-ol; 2- (3-amino pyrazolo- [1, 5-a] -pyrimidin-7-ylamino) -ethanol, 2- (7-amino pyrazolo- [1, 5 a] -pyrimidin-3-ylamino) - ethanol, 2 - [(3-amino-pyrazolo [1, 5-a] pyrimidin-7-yl) -

(2-hydroxy-ethyl) -amino] -ethanol, 2 - [(7-amino-pyrazolo [1, 5-a] pyrimidin-3-yl) - (2-hydroxy-ethyl) -amino] -ethanol, 5,6-dimethyl pyrazolo- [1,5-a] -pyrimidine-3,7-diamine, 2,6-dimethyl pyrazolo- [1,5-a] -pyrimidine-3,7-diamine, 2 , 5, N 7, N 7- tetramethyl pyrazolo- [1,5-a] -pyrimidine-3,7-diamine, 3-amino-5-methyl-7-imidazolylpropylamino pyrazolo- [1,5-a] - pyrimidine and their acid addition salts and their tautomeric forms, when there is a tautomeric equilibrium. Among the pyrazole derivatives, mention may more particularly be made of the compounds described in patents DE 3 843 892, DE 4 133 957 and patent applications WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 195 43 988 such as 4,5-diamino 1-methyl pyrazole, 4,5-diamino 1 - (β-hydroxyethyl) pyrazole, 3,4-diamino pyrazole, 4,5-diamino 1- (4'-chlorobenzyl) pyrazole, 4,5-diamino 1, 3-dimethyl pyrazole, 4,5-diamino 3-methyl 1-phenyl pyrazole, 4,5-diamino 1-methyl 3-phenyl pyrazole, 4-amino 1, 3 -dimethyl 5-hydrazino pyrazole, 1-benzyl 4,5-diamino 3-methyl pyrazole, 4,5-diamino 3-tert-butyl 1-methyl pyrazole, 4,5-diamino 1-tert-butyl 3- methyl pyrazole, 4,5-diamino 1 - (β-hydroxyethyl) 3-methyl pyrazole, 4,5-diamino 1 -ethyl 3- methyl pyrazole, 4,5-diamino 1 -ethyl 3- (4'- methoxyphenyl) pyrazole, 4,5-diamino 1-ethyl 3-hydroxymethyl pyrazole, 4,5-diamino 3-hydroxymethyl 1-methyl pyrazole, 4,5-diamino 3-hydroxymethyl 1-isopropyl pyrazole, 4,5-diamino 3-methyl 1-isopropyl pyrazole, 4-amino 5- (2'-aminoethyl) amino 1,3-dimethyl pyrazole, 3, 4,5-triamino pyrazole, 1-methyl 3,4,5-triamino pyrazole, 3,5-diamino 1-methyl 4-methylamino pyrazole, 3,5-diamino 4- (β-hydroxyethyl) amino 1- methyl pyrazole, and their addition salts with an acid.

When they are used, the additional oxidation base (s) preferably represent from 0.0001 to 10% by weight approximately of the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight approximately of this weight . In general, the addition salts with an acid which can be used in the context of the dye compositions of the invention (oxidation bases and couplers) are in particular chosen from hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, phosphates and acetates. The addition salts with a base which can be used in the context of the dye compositions of the invention are in particular those obtained with soda, potash, ammonia or amines.

The dye composition in accordance with the invention may also contain one or more direct dyes which can in particular be chosen from nitro dyes of the benzene series, cationic direct dyes, in particular azo or methine dyes.

The dye composition in accordance with the invention may also contain various adjuvants conventionally used in compositions for dyeing the hair, such as anionic, cationic, nonionic, amphoteric, zwitterionic surfactants or mixtures thereof, anionic polymers, cationic, non-ionic, amphoteric, zwitterionic or mixtures thereof, mineral or organic thickening agents, and in particular associative anionic, cationic, nonionic and amphoteric polymeric thickeners, antioxidant agents, penetration agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such as for example volatile or non-volatile silicones, modified or unmodified, film-forming agents, ceramides, preserving agents, opacifying agents.

These compounds can be present in an amount of between 0.01 and 20% by weight of the total weight of the composition.

Of course, those skilled in the art will take care to choose this or these optional additional compounds in such a way that the advantageous properties intrinsically attached to the oxidation dye composition in accordance with the invention are not or substantially not altered by the addition (s) envisaged.

The dye composition according to the invention can be in various forms, such as in the form of liquids, creams, gels or in any other form suitable for dyeing keratin fibers, and in particular human hair.

The subject of the invention is also a process for dyeing keratin fibers and in particular human keratin fibers such as the hair using the dye composition as defined above.

According to this method, at least one dye composition as defined above is applied to the fibers, the color being revealed using an oxidizing agent. The color can be revealed at acidic, neutral or alkaline pH and the oxidizing agent can be added just at the time of use to the dye composition or in an oxidizing composition applied simultaneously or sequentially.

According to a preferred embodiment of the dyeing method of the invention, the dye composition described above is preferably mixed with a composition containing, in a medium suitable for dyeing, at the time of use. minus an oxidizing agent present in an amount sufficient to develop coloring. The mixture obtained is then applied to the keratin fibers. After an exposure time of 3 to 50 minutes approximately, preferably 5 to 30 minutes approximately, the keratin fibers are rinsed, washed with shampoo, rinsed again and then dried.

The oxidizing agent can be chosen from the oxidizing agents conventionally used for the oxidation dyeing of keratin fibers, and among which mention may be made of hydrogen peroxide, urea peroxide, alkali metal bramates, persalts such as as perborates and persulfates, peracids and enzymes among which mention may be made of peroxidases, 2-electron oxidoreductases such as uricases and 4-electron oxygenases such as laccases. Hydrogen peroxide is particularly preferred.

The pH of the oxidizing composition containing the oxidizing agent is such that after mixing with the dye composition, the pH of the resulting composition applied to the keratin fibers preferably varies between 3 and 12 approximately, and even more preferably between 5 and 11 It can be adjusted to the desired value at means of acidifying or basifying agents usually used in dyeing keratin fibers and as defined above.

The oxidizing composition as defined above may also contain various adjuvants conventionally used in compositions for dyeing the hair and as defined above.

The composition which is finally applied to the keratin fibers can be in various forms, such as in the form of liquids, creams, gels, or in any other form suitable for dyeing keratin fibers, and in particular human hair. . Another object of the invention is a device with several compartments or

Dye "kit" in which a first compartment contains the dye composition defined above and a second compartment contains the oxidizing composition. This device can be equipped with a means enabling the desired mixture to be delivered to the hair, such as the devices described in patent FR-2,586,913 in the name of the applicant.

The subject of the invention is finally the colored product capable of being obtained by reaction of the base of formula (I) as defined above and the forum coupler (III) as defined above. This colored product can be used in cosmetic products, for example make-up. The following examples are intended to illustrate the invention.

DYEING EXAMPLES

Examples 1: Staining in Basic Medium

The following dye composition was prepared, according to the invention:

At the time of use, this weight-for-weight composition is mixed with hydrogen peroxide titrating 20 volumes (6% by weight), of pH 3. This mixture is applied to locks of natural gray hair containing 90% white hairs. . After 30 min. laying, the locks are rinsed, washed with shampoo, rinsed again and dried. The hair is dyed in the shades described below.

Example 2. Staining in a neutral medium pH = 7

The following dye composition was prepared according to the invention

At the time of use, this weight-for-weight composition is mixed with hydrogen peroxide titrating 20 volumes (6% by weight), of pH 3. The pH of the mixture is 7. This mixture is applied to gray hair 90% natural whites. After 30 min. laying, the locks are rinsed, washed with shampoo, rinsed again and dried. The hair is dyed in the shades described below.

EXAMPLE 3 Staining at pH 7 with the Q ₂ / Laccase Development System

The following dye composition was prepared according to the invention

Pyrazolo [1,5-a] pyridin-3-ylamine monochlorohydrate 0.509 g

6-methoxy-2,3-diaminopyridine 0.636 g hydroxyethyl cellulose (MW: 1,300,000) 1.5 g carboxymethyl chitosan 2 g polyglycerol monooleate 1 g

This mixture is applied to natural gray hair with 90% white. After 30 min. laying, the locks are rinsed, washed with shampoo, rinsed again and dried. The hair is dyed with a matt ash reflection.

Claims

1. Composition for the oxidation dyeing of keratin fibers, characterized in that it comprises, in a suitable medium for dyeing,

in which :

- Ri, R ₂ , R ₃ , R ₄ and R ₅ , identical or different, represent a hydrogen or halogen atom; a radical -NHSO ₃ H; a hydroxyl radical; an alkyl radical; an alkoxy radical; an alkylthio radical; an amino radical; a monoalkylamino radical; a dialkylamino radical in which the two alkyl groups can, together with the nitrogen atom to which they are linked, form a ring which can be interrupted by one or more nitrogen, oxygen or sulfur atoms; a heterocycle; a nitro radical; an aryl radical; a C1-C4 acyl radical; an alkoxy (CrC ₄ ) carbonyl radical; a carboxamido radical; a cyano radical; a radical - CO ₂ H, a radical -SO ₃ H; a radical -P0 ₃ H ₂ ; a radical -PO ₄ H ₂ ; or a group of the following formula (II):

in which X and R independently of one another represent an oxygen atom, an NH or N (CrC) alkyl group, and Y represents a hydroxyl, amino, alkyl, alkoxy, alkylamino, or dialkylamino radical, and “ at least one diamino or triamino pyridine coupler of formulas (III), (IV) or (V) below: in which

- R7 and RIO, identical or different, represent a hydrogen atom; an alkyl radical,

2. Composition according to claim 1, characterized in that the compounds of formula (I) are chosen from the compounds of formula (la) below, and their addition salts with an acid or with a base:

in which :

Ri, R ₂ , R3, identical or different, represent a hydrogen or halogen atom; a radical -NHSO ₃ H; a hydroxyl radical; an alkyl radical; an alkoxy radical; an alkylthio radical; an amino radical, a monoalkylamino radical; a dialkylamino radical in which the two alkyl groups can, together with the nitrogen atom to which they are linked, form a ring which can be interrupted by one or more nitrogen, oxygen or sulfur atoms; a heterocycle; an acyl radical; an alkoxycarbonyl radical; a carboxamido radical; or a group of the following formula (II) in which X and R independently of one another represent an oxygen atom, an NH or N (CC ₄ ) alkyl group, and Y represents a hydroxyl, amino, alkyl, alkoxy, alkylamino, or dialkylamino radical.

3. Composition according to claim 1 or 2 in which the 3-amino pyrazolo- [1,5-a] -pyridines of formula (I) are chosen from:

- pyrazolo [1,5-a] pyridin-3-ylamine;

- 2-acetylamino pyrazolo- [1,5-a] pyridin-3-ylamine;

- 2-methoxy-pyrazolo [1,5-a] pyridine-3-ylamino;

- (3-amino-pyrazolo [1,5-a] pyridine-7-yl) -methanol;

- 2- (3-amino-pyrazolo [1,5-a] pyridine-5-yl) -ethanol;

- 2- (3-amino-pyrazolo [1,5-a] pyridine-7-yl) -ethanol; - (3-amino-pyrazolo [1,5-a] pyridine-2-yl) -methanol;

- 3,6-diamino-pyrazolo [1,5-a] pyridine;

- 3,4-diamino-pyrazolo [1,5-a] pyridine;

- pyrazolo [1,5-a] pyridine-3,7-diamine;

- 7-morpholin-4-yl-pyrazolo [1, 5-a] pyridin-3-ylamine; - pyrazolo [1,5-a] pyridine-3,5-diamine;

- 5-morpholin-4-yl-pyrazolo [1, 5-a] pyridin-3-ylamine;

- 2 - [(3-amino-pyrazolo [1,5-a] pyridin-7-yl) - (2-hydroxyethyl) -amino] -ethanol;

- 3-amino-pyrazolo [1,5-a] pyridine-5-ol; - 3-amino-pyrazolo [1,5-a] pyridine-4-ol;

- 3-amino-pyrazolo [1,5-a] pyridine-6-ol;

- 3-amino-pyrazolo [1,5-a] pyridine-7-ol; and their addition with an acid or with a base.

4. Composition according to any one of the preceding claims, characterized in that the 3-amino pyrazolo- [1, 5-a] -pyridines of formula (I) and / or the addition salt or salts thereof with a acid or a base represent from 0.0001 to 10% by weight of the total weight of the dye composition.

5. Composition according to Claim 4, characterized in that the 3-amino pyrazolo- [1, 5-a] -pyridines of formula (I) and / or the addition salt or their salts with an acid or a base represent from 0.005 to 6% by weight of the total weight of the dye composition. 6. Composition according to any one of claims 1 to 5 in which the coupler of formula (III), (IV) or (V) is chosen from 2,6-dimethoxy-3,5-diaminopyridine; 6-methoxy-N2-methyl-2,3-diaminopyridine; 6-methoxy-2,3-diaminopyridine; the 2,

6-diamino-pyridine.

7. Composition according to any one of the preceding claims, characterized in that the coupler of formula (III), (IV) or (V) is present in an amount between 0.0001 to 10% by weight approximately of the total weight of the dye composition.

8. Composition according to any one of the preceding claims, further comprising at least one additional oxidation base chosen from paraphenylenediamines, bis-phenylalkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases other than 3- amino pyrazolo- [1,5-a] -pyridines of formula (I) as defined in claim 1.

9. Composition according to any one of the preceding claims, further comprising one or more additional couplers chosen from metaphenylenediamines, meta-aminophenols, metadiphenols, naphthalene couplers and heterocyclic couplers.

10. Composition according to claim 9, characterized in that the additional couplers are chosen from 2-methyl 5-aminophenol, 5-N- (β-hydroxyethyl) âmino 2-methyl phenol, 6-chloro-2-methyl ~ 5-aminophenol, 3-amino phenol, 1, 3-dihydroxy benzene, 1, 3-dihydroxy 2-methyl benzene, 4-chloro 1, 3-dihydroxy benzene, 2,4-diamino l- ( β-hydroxyethyloxy) benzene, 2-amino 4- (β- hydroxyethylamino) 1-methoxybenzene, 1,3-diamino benzene, 1, 3-bis- (2,4-diaminophenoxy) propane, 3-ureido aniline , 3-ureido 1-dimethylamino benzene, sesamol, 1-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2 methyl-1-naphthol, 6-hydroxy indole, 4-hydroxy indole, 4-hydroxy N-methyl indole, 6-hydroxy benzomorpholine, 2-amino-3-hydroxy pyridine, 1-N- (β-hydroxyethyl) amino-3,4-methylene dioxybenzene, 2,6 -bis- (β- hydroxyethylamino) toluene and their addition salts.

11. Process for the oxidation dyeing of keratin fibers, characterized in that at least one dye composition as defined in any one of claims 1 to 10 is applied to the fibers, and the color is revealed by presence of an oxidizing agent.

12. The method of claim 11, characterized in that the oxidizing agent is chosen from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts, peracids, and enzymes.

13. Multi-compartment device comprising a first compartment which contains a dye composition as defined in any one of claims 1 to 10 and a second compartment which contains a composition containing an oxidizing agent.

14. Colored product capable of being obtained by reaction of an oxidation base of formula (I) and of a coupler of formula (III), (IV) or (V) from the composition according to one any of claims 1 to 10.