EP1339693A1

EP1339693A1 - Diaminopyrazole derivatives and their use for oxidation dyeing of keratinous fibres

Info

Publication number: EP1339693A1
Application number: EP01999561A
Authority: EP
Inventors: Thilo Fessmann; Eric Terranova
Original assignee: LOreal SA
Current assignee: LOreal SA
Priority date: 2000-12-06
Filing date: 2001-11-29
Publication date: 2003-09-03
Also published as: US7250063B2; JP2004515495A; FR2817551B1; US20040083558A1; FR2817551A1; WO2002046165A1; AU2002222074A1; KR20030070046A; AR031774A1; MXPA03005029A; CN1478079A; BR0116190A

Abstract

The invention concerns novel diaminopyrazole derivatives of formula (I), wherein: R1 represents C1-C6 alkyl or C2-C6, preferably up to C4, alkenyl, linear or branched, bearing at least a substituent selected among OR, NHR, NRR', SR, SO2R, COOH, CONH2, CONRR', PO(OH)2, SH, SO3X, a non-cationic heterocycle, Cl, Br or I; X represents H, Na, K or NH4; R and R', identical or different, represent C1-C6 alkyl or C2-C6, preferably up to C4, alkenyl, linear or branched, unsubstituted or substituted by one or several functional groups selected among OH, NH2, OR, NHR, NRR', SR, SOR, SO2R, COOH, CONH2, CONRR', PO(OH)2, SH, SO3X, a non-cationic heterocycle, Cl, Br or I, X, R and R' having the definitions mentioned above; R2 represents H, or C1-C6 alkyl or C2-C6, preferably up to C4, alkenyl, linear or branched, unsubstituted or substituted by one or several functional groups selected among OH, NH2, OR, NHR, NRR', SR, SOR, SO2R, COOH, CONH2, CONRR', PO(OH)2, SH, SO3X, a non-cationic heterocycle, Cl, Br or I, X, R and R' having the definitions mentioned above; and their physiologically acceptable salts, and their use for oxidation dyeing of keratinous fibres, in particular human hair.

Description

DIAMINOPYRAZOLE DERIVATIVES AND THEIR USE IN OXIDATION DYES OF KERATINIC FIBERS

The present invention relates to new diaminopyrazole derivatives, to a composition for the oxidation dyeing of keratin fibers, and in particular human keratin fibers such as the hair, comprising at least, as oxidation base, a derivative of diaminopyrazole and to the oxidation dyeing processes using it.

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 para-aminophenols, heterocyclic compounds such as derivatives diaminopyrazole, generally called oxidation bases. The precursors of oxidation dyes, or 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.

We also know that we can vary the nuances obtained with these oxidation bases by associating them with couplers or color modifiers, the latter being chosen in particular from aromatic metadiamines, meta-aminophenols, metadiphenols and certain compounds. heterocyclic.

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

The so-called "permanent" coloration obtained by means of 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 exhibit 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 sensitized differently (that is to say damaged) between its tip and its root. They must also have good chemical stability in the formulations. They must have a good toxicological profile.

In addition, for a certain number of applications, dyes are sought which give chromatic nuances to the hair.

We know from patent applications DE 42 34 885, 196 43 059 and

196 46 609 derivatives of 4,5-diaminopyrazole which, when used in conjunction with different couplers, in particular benzoxazines, give chestnut-like nuances with blue, red, purple, aubergine or coppery highlights.

However, these dyes do not meet all of the above requirements.

Now, the Applicant has now discovered, in a totally unexpected and surprising manner, that it was possible to obtain dyes, capable of leading to powerful colorings, particularly chromatic and brilliant, not very selective, and having excellent properties of resistance to various aggressions that keratin fibers can undergo. using the diaminopyrazoles of formula (I) below or their physiologically acceptable salts as the oxidation base.

The subject of the present invention is therefore the new diaminopyrazoles having the following structure:

in which

Ri denotes a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C, linear or branched, carrying at least one substituent chosen from OR, NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH ₂ , CONRR ', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I,

X denotes H, Na, K or NH ₄ ,

R and R ', identical or different, denote a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more chosen functional groups among OH, NH ₂ , OR,

NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH _2, CONRR', PO (OH) _2, SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X, R and R ' having the definitions indicated above,

R ₂ denotes H, or a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more functional groups chosen from OH, NH ₂ , OR, NHR, NRR ', SR,

SOR, S0 ₂ R, COOH, CONH ₂ , CONRR *, PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X, R and R 'having the definitions indicated above .

A subject of the invention is also the physiologically acceptable acid or base salts of the compounds of formula (I) such as the hydrochlorides, hydrobromides, sulfates, tartrates, lactates or acetates, or the salts obtained with the soda, potash, ammonia or amines or alkanolamines.

The subject of the invention is also a composition for the oxidation dyeing of keratin fibers, and in particular human keratin fibers such as the hair, characterized in that it contains, in a medium suitable for dyeing, at least as an oxidation base a diaminopyrazole of formula (I) above, or its physiologically acceptable acid or base salts.

As indicated above, the colors obtained with the oxidation dye composition in accordance with the invention are powerful, particularly bright and chromatic. They make it possible in particular to obtain shades free or containing very little blue or yellow. They also have excellent resistance properties vis-à-vis the action of various external agents (light, bad weather, washing, permanent waving, perspiration, friction).

The subject of the invention is also a process for the oxidation dyeing of keratin fibers using such a dye composition.

As examples of diaminopyrazoles of formula (I) according to the invention, mention may be made of the compounds belonging to the following classes:

According to a preferred embodiment of the invention in formula (I), Ri is a linear Cι-C ₃ alkyl radical, substituted by a group S0 ₃ H, COOH, CONH ₂ , methoxy, 2-hydroxyethyloxy, 2- hydroxyethylamino, mono- or dimethylamino, pyrrolidin-1-yle -3-ol, imidazolidin-1-yle, pipérazin-1-yle, pipérazin-1-yl-ethanol, tetrahydrofuran-2-yle or tetra ydropyran-2-yle and R ₂ denotes H, methyl, ethyl, 2-hydroxyethyl, 2-methoxyethyl, 2-aminoethyl or carboxymethyl. The diaminopyrazoles of formula (I) preferred according to the invention have the following structures:

The diaminopyrazoles of formula (I) more particularly preferred according to the invention are 4,5-diamino-l- (2'-methoxyethyl) -ρyrazole and 4-amino- l- (2'-methoxyethyl) -5-methylamino pyrazole or their addition salts with physiologically acceptable acids. The diaminopyrazoles of formula (I) according to the invention are prepared for example according to the following general method of preparation:

The synthetic approach shown below is described in the literature up to intermediary (2) (JHP Juffermanns, C. L-; Habraken; J. Org. Chem., 1986, 51, 4656; Klebe et al. ; Synthesis, 1973, 294; R. Hϋttel, F. Bϋchele; Chem. Ber.; 1955, 88, 1586.).

The alkylation and amination to arrive at the compounds of type (5) of formula (I) according to the invention are mentioned in document DE 42 34 885.

1) HNOJΗOAc 2) toluene, Δ

Examples of synthesis:

Synthesis of 3,4.5-tribromopyrazole (1):

NaOH (24 g, 0.6 mole) was added to an aqueous pyrazole solution (10 g, 0.147 mole) with stirring (the temperature of the reaction medium rose to 35 ° C). After cooling the reaction medium to 20 ° C, Br ₂ (72 g, 0.45 mole) was added dropwise for 1 h while maintaining the temperature between 20 ° C and 25 ° C. The reaction was followed by TLC or thin layer chromatography (50% Hexane / 50% AcOEt or ethyl acetate). The precipitate was filtered and washed with demineralized water (100 ml). The filtrate was acidified to pH 6-7 using HCl (10%, 33 g, 0.27 mole) and keeping the temperature between 20 and 25 ° C. The precipitate thus formed is filtered and washed with demineralized water (100 ml). The combined solids are brought to reflux in a Dean-Stark apparatus in the presence of toluene (200 ml). At the end of the water collection, the organic phase is filtered hot. The solvent is evaporated to a residual volume of 110 ml. The solution is cooled to 0-5 ° C for 1 h. The precipitate formed is collected by filtration, washed with cold toluene (20 ml) and dried under vacuum at 80 ° C to give the tribromide (1) in the form of an off-white solid (30 g, 67%).

NMR: 13C (100 MHz, d6-DMSO): 97.7, 116.1, 126.4

IR (KBr; cm-1): 3100, 2861, 1531, 1356, 1019, 969

M.p .: 182-184 ° C

Synthesis of 3.5-dibromo-4-nitropyrazole (2): HN0 ₃ (d = 1.50 g / ml; 18 ml, 0.429 mole) was added dropwise for 10 min to a solution of 3,4,5- tribromopyrazole (50 g, 0.164 mole) in glacial acetic acid (750 ml) while maintaining the temperature at 15 ° C. Acetic anhydride (250 ml) was added and the reaction mixture was stirred at room temperature for 2 h. After complete reaction, the reaction mixture was poured onto broken ice (1 kg). After 1 h of stirring, the crude product was filtered, then washed with demineralized water (2 x 60 ml) to give crude l-nitro-3,4,5-tribromopyrazole. The water (24.6 ml) contained in the wet product was removed by heating a solution of the product in toluene (750 ml) at reflux in a Dean-Stark apparatus. The toluene solution was held at reflux for an additional 30 min until a TLC

(eluent toluene) indicates that the rearrangement of l-nitro-3,4,5-tribromopyrazole

(Rf = 0.77), intermediate formed, in 3,5-dibromo-4-nitropyrazole 2 (Rf = 0.05) is complete. The solution was concentrated to a residual volume of

150 ml, then allowed to cool to 60 ° C before adding hexane (275 ml). The solution was cooled to 0-5 ° C for 1 h and 3,5-dibromo-4-nitropyrazole 2 (29.1 g, 65%) was collected by filtration and drying under vacuum as a yellow solid clear.

IR (KBr, cm-1): 3211, 1541, 1441, 1370, 1334, 976, 960, 824

M.p .: 127.6-130.1 ° C.

General method of synthesis of alkyl-3.5-dibromo-4-nitropyrazole (3): A solution of 3,5-dibromo-4-nitropyrazole (2) (1 mmol) in DMF or dimethylformamide (4.8 ml) was added dropwise to a solution of NaH (1.1 mmol; dispersion in oil at 60% previously washed with hexane under an inert atmosphere) in DMF (8 ml) with stirring. A release of hydrogen gas occurs. After 30 minutes, a solution of alkyl halide (1.2 mmol) in DMF (1.6 ml) was added dropwise for

10 min followed by heating the reaction medium at 50-60 ° C for 3 h (followed by TLC). The DMF was evaporated under reduced pressure and the residue is taken up in a mixture of DCM or dichloromethane (4 ml) and water (10 ml). The aqueous phase was extracted with DCM (3 x 10 ml) and the combined organic phases are washed with water (50 ml). The organic phase was dried over

MgS0 and the solvent was evaporated under reduced pressure to give the alkylated products of type (3) in the form of oils or solids. The products were used without further purification in the amination step.

General method of synthesis of 1-alkyl-5-alkylamino-3-bromo-4-nitropyrazole (4):

A mixture of 1-alkyl-3,5-dibromo-4-nitropyrazole (1 mmol) and alkylamine

(14 ml) in ethanol (25 ml) was heated at reflux for 4 h (followed by TLC). Ethanol and excess alkylamine were evaporated under reduced pressure. After trituration of the reaction crudes with isopropyl ether, the compounds of type (4) are obtained as solids. S ynth è se of S-bromo-l - ^ '- methoxyethvD-S-methylamino ^ - nitropyrazole (type 4 compound):

A 40% aqueous solution of methylamine (300 ml, 8.71 moles) is added to a solution of 3,5-dibromo-1- (2'-methoxyethyl) -4-nitropyrazole (15 g,

0.483 mol) in ethanol (300 ml). The reaction mixture was stirred at 20-25 ° C for 2 h, then cooled to 0-5 ° C for 30 min. The precipitate formed was filtered and washed with a cold mixture of water / ethanol (1/1, 30 ml). The final amine product was obtained in the form of a yellow solid (4.6 g, 36%) after drying under reduced pressure.

TLC (1/1: Hexane / ethyl acetate): R _f = 0.31 PF: 154.4-156.8 ° C

IR (KBr, cm-1): 3336, 1625, 1541, 1473, 1446, 1338,

1239, 1049, 839 NMR: 1 H (400 MHz, d ⁶ -DMSO): 4.27 (2 H, t, J = 5.0 Hz, CH ₂ N),

3.74 (2H, t, J = 5.0 Hz, CH ₂ 0), 3.34 (3 H, s, OCH ₃ ), 3.24 (3 H, d, J = 5.5 Hz, CH ₃ N).

Synthesis of 3-bromo-1- ( ^' 2'-methoxyethylV5-benzylamino-4-nitro-pyrazole (type 4 compound):

. The general method is applied using benzylamine. The final amine product was recrystallized from a MeOH / H ₂ O mixture (1/1) and was isolated as a yellow solid (48%).

TLC (1/1: Hexane / ethyl acetate): R _f = 0.46 PF: 91.1-93.8 ° C

IR (KBr; cm ^-1 ): 3333, 1602, 1583, 1536, 1469,

1410, 1332, 1296, 1229, 1106, 1060, 732 NMR: 1H (400 MHz, CDC1 ₃ ): 7.34 (5H, m, H ^), 4.77 (2H, d,

J = 6.5 Hz, NHCHb), 4.11 (2 H, t, J = 5.0 Hz, CH ₂ N), 3.71 (2 H, t, J = 5.0 Hz, CH ₂ 0 ), 3.34 (3 H, s, OCH ₃ ). ^"

4-amino-1- (2'-methoxyethyl -5-methylaminopyrazole dihydrochloride (type 5 compound) or (I):

A mixture of 3-bromo-1- (2'-methoxyethyl) -5-methylamino-4-pyrazole (5 g, 18 mmol) in ethanol (500 ml) containing a 10% Pd / C catalyst (Johnson- Mattey Type 487, dry weight 0.5 g) and 36% hydrochloric acid (4.1 g, 40.4 mmol) was hydrogenated in a Parr Autoclave (1 1) at 1.1 MPa for 3 h (followed by TLC ). The catalyst was removed by filtration, washed with ethanol and the filtrate was evaporated under reduced pressure. Under an inert atmosphere, the crude oil was taken up in ethanol (80 ml) and was heated to 50 ° C. AcOEt (80 ml) was added and the mixture was kept at room temperature for 3 h, then cooled to 0-5 ° C for 2 h. The precipitate was recovered by filtration, washed with a cold mixture of EtOH / AcOEt (1/1, 2 x 30 ml) and dried under vacuum to give the dihydrochloride of the final diamine in the form of an off-white solid (4, 1 g, 93%).

HPLC (purity): 99.5% TLC (MeOH): R _f = 0.57 (colorless spot turning red in contact with oxygen)

M.p .: 157.6-159.8 ° C

IR (KBr, cm ^-1 ): 3237, 3128, 2760, 2546, 1621, 1112

NMR: 1H (400 MHz, d ⁶ -DMSO): 7.46 (1H, s, NH ^), 4.10 (2H, t,

J = 5.5 Hz, CH ₂ N), 3.62 (2 H, t, J = 5.5 Hz, CH ₂ 0), 3.22 (3 H, s, OCH ₃ ), 2.84, (3 H, s, NCH ₃ ).

4,5-Diamino-l- (2'-methoxyethylVpyrazole dihydrochloride (type 5 compound) or (I):

A mixture of 5-benzylamino-3-bromo- l- (2'-methoxyethyl) -4- nitropyrazole (4 g, 2.8 mmol) in ethanol (500 ml) containing a 10% Pd / C catalyst ( Johnson-Mattey Type 487, dry weight 0.5 g) and 36% hydrochloric acid (0.57 g, 5.6 mmol) was hydrogenated in a Pair Autoclave (1 1) at 1 MPa for 1 h (followed by TLC ). The catalyst was removed by filtration, washed with ethanol and the filtrate was evaporated under reduced pressure. A crude orange solid (2.8 g, 108%) is obtained which has been triturated in AcOEt (20 ml) for 1 h. The solid was filtered and washed with cold AcOEt (20 ml) then dried under vacuum to give the diamine (type 5) in the form of a beige solid (0.7 g, 27%).

HPLC (purity): 99.5% TLC (MeOH): R _f = 0.48 (colorless spot turning red in contact with oxygen)

M.p .: 168.1-173.0 ° C

IR (KBr, cm-1) 3309.3158,3050,2892,1647,

1619, 1587, 1504, 1422, 1344,

1281.1111

NMR: 1H (400 MHz, d ⁶ -DMSO) 7.34 (1H, s, NH _arom ), 5.18 (1H,

S _l a _rge , NH), 4.09 (2H, t, J = 5.5

Hz, CH ₂ N), 3.61 (2H, t, J = 5.5 Hz, CH ₂ 0), 3.23 (3 H, s, OCH ₃ ).

The dye composition according to the invention contains in particular from 0.001 to 10% by weight, preferably from 0.05 to 6% by weight, and even more preferably from 0.1 to 3% by weight, of at least one diaminopyrazole of formula (I) or its salts.

The dye composition in accordance with the invention can also contain, in addition to (or) diaminopyrazole (s) defined above, at least one additional oxidation base which can be chosen from the oxidation bases conventionally used in oxidation dyeing and among which there may be mentioned in particular paraphenylenediamines, bis-phenylalkylenediamines, para-aminophenols, ortho-aminophenols and heretocyclic bases other than 4,5-diaminopyrazole used. Among the paraphenylenediamines, mention may more particularly be made, for example, of paraphenylenediamine, paratoluylenediamine, 2,6-dimethyl paraphenylenediamine, 2-β-hydroxyethyl paraphenylenediamine, 2-n-propyl paraphenylenediamine, 2-isopropyline paraphenyl , N- (β- hydroxypropyl) paraphenylenediamine, N, N-bis- (β-hydroxyethyl) paraphenylenediamine, 4-amino N- (β-mehoxyethyl) aniline, the paraphenylenediamines described in French patent application FR 2630438, and their addition salts.

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-diaminopropanol, N, N'-bis- (β-hydroxyethyl) N, N'-bis- (4'-aminophenyl) ethylene diamine, N, N'-bis- (4-amino phenyl) tetra-methylenediamine, N, N'- bis- (β-hydroxyethyl), N, N'-bis- (4-aminophenyl) tetramethylenediamine, N, N'- bis- (4-methylaminophenyl) tetramethylene diamine, N, N'-bis- (ethyl) N, N'-bis-

(4'-amino, 3'-methylρhenyl) ethylenediamine, and their addition salts.

Among the para-aminophenols, there may be mentioned more particularly by way of example, para-aminophenol, 4-amino 3-methyl phenol, 4-amino 3-fluoro phenol, 4-amino 3-hydroxy-methyl 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 , and their addition salts.

Among the ortho-aminophenols, mention may more particularly be made, by way of example, of 2-amino phenol, 2-amino 5-methyl phenol, 2-amino-6-methylphenol, 5-acetamido 2-amino phenol, and their addition salts.

Among the heterocyclic bases that may be mentioned more particularly by way of example, pyridine derivatives, pyrimidine derivatives, pyrazole derivatives other than the diamino pyrazoles of formula (I) used in accordance with the invention, and their addition salts. When used, these additional oxidation bases preferably represent from 0.0005 to 12%) by weight of the total weight of the dye composition, and even more preferably from 0.005 to 6% by weight of this weight.

The oxidation dye compositions in accordance with the invention may also contain at least one coupler and / or at least one direct dye, in particular for modifying the nuances or enriching them with reflections.

The couplers which can be used in the oxidation dye compositions in accordance with the invention can be chosen from the couplers conventionally used in oxidation dyeing and among which there may be mentioned in particular metaphenylenediamines, meta-aminophenols, metadiphenols, mono or polyhydroxy derivatives of naphthalene and heterocyclic couplers such as, for example, indole or pyridine derivatives and their addition salts.

These couplers are more particularly chosen from 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, l, 3-bis- (2,4-diaminophenoxy) propane, 3-ureido aniline, 3-ureido 1-dimethylamino benzene, sesamol, l-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2 methyl-1 naphthol, 6-hydroxy indole, 4-hydroxy indole, 4-hydroxy N-methyl indole, 2-amino-3-hydroxy pyridine, 6-hydroxy benzomorpholine 3,5-diamino-2,6-dimethoxypyridine, 1 -N- (β-hydroxyethyl) amino-3,4-methylene dioxybeήzene, 2, 6-bis- (β-hydroxyethylamino) toluene and their addition salts.

When they are present, these couplers represent in particular from 0.0001 to 10% of the total weight of the dye composition, preferably from 0.005 to 5% by weight, and even more preferably from 0.1 to 3% 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, sulfates, tartrates, lactates and acetates. The addition salts with a base are especially those obtained with soda, potash, ammonia, amines or alkanolamines.

The medium suitable for dyeing (or support) used according to the invention consists of water or of a mixture of water and at least one organic solvent chosen from lower C ₁ -C ₄ alkanols, polyols and polyol ethers, aromatic alcohols, analogues and their mixtures.

The dye composition according to 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, cationic polymers , non-ionic, amphoteric, zwitterionic or their mixtures, mineral or organic thickening agents, antioxidant agents, reducing agents, sun filters, penetration agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such as, for example, silicones, film-forming agents, preserving agents, opacifying agents.

The pH of the dye composition according to the invention is between 3 and 12.

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 according to the invention are not, or not substantially, 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 under any other suitable form 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 process, at least one dye composition as defined above is applied to the fibers, for a time sufficient to develop the desired coloration, either in air or using an oxidizing agent. The dye composition may optionally contain oxidation catalysts, in order to accelerate the oxidation process.

According to a first embodiment of the process of the invention, the coloring of the fibers can be carried out without the addition of an oxidizing agent, only in contact with the oxygen in the air.

According to a second embodiment of the process of the invention, at least one dye composition as defined above is applied to the fibers, the color being revealed at acidic, neutral or alkaline pH using an oxidizing agent which is added just at the time of use to the dye composition or which is present in an oxidizing composition applied simultaneously or sequentially separately.

According to this second form of implementation of the dyeing process of the invention, the dye composition described above is preferably mixed with an oxidizing composition containing, in a medium suitable for dyeing, at the time of use, at least one oxidizing agent present in an amount sufficient to develop coloring. The mixture obtained is then applied to the keratin fibers and left to stand for 3 to 50 minutes, preferably 5 to 30 minutes, after which it is rinsed, washed with shampoo, rinsed again and dried. The oxidizing agent present in the oxidizing composition as defined above 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, peroxide of urea, alkali metal bromates, persalts such as perborates and persulfates. Hydrogen peroxide is particularly preferred.

The pH of the oxidizing composition containing the oxidizing agent as defined above 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, and even more preferably between 5 and 11. It is adjusted to the desired value by 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 "kit" for dyeing or any other packaging system with several compartments, a first compartment of which contains the dye composition as defined above and a second compartment of which contains the oxidizing composition. as defined above. These devices 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 following examples are intended to illustrate the invention. EXAMPLES 1 TO 4 (dyes in an alkaline medium

The following coloring formulations are produced:

- 4, 5 -diaminopyrazole 5 x 10 ^"3 mole

- Coupler 5 x 10 ^"3 mole

- Polyglycerole oleic alcohol with 2 moles of glycerol 4.0 g

- Polyglycerole oleic alcohol with 4 moles of glycerol with 78% of active ingredients (M.) 5.7 g MA.

- Oleic acid 3.0 g

- Oleic amine containing 2 moles of ethylene oxide sold under the trade name ETHOMEEN 012 by the company AKZO 7.0 g - Laurylamino diethylaminopropyl succinamate, sodium salt at 55% of MA. 3.0 g MA.

- Oleic alcohol 5.0 g

- Oleic acid diethanolamide 12.0 g

- Propylene glycol 3.5 g - Ethyl alcohol 7.0 g - Dipropylene glycol 0.5. g

- Propylene glycol monomethyl ether 9.0 g

- Sodium metabisulfite in aqueous solution at 35% of MA. 0.455g MA. - Ammonium acetate 0.8 g

- Antioxidant, sequestering q.s.

- Perfume, preservative q.s.

- Ammonia at 20% NH3 100 g pH = 9.5 MA. means "active ingredient"

At the time of use, each weight-for-weight dye composition is mixed with a solution of hydrogen peroxide at 20 volumes (6% by weight), the pH of which has been adjusted to approximately 2.5 with orthophosphoric acid.

The mixture is applied to gray hair with 90% white, natural or permanent, at a rate of 5 g for 0.5 g of hair, for 30 min.

The hair is then rinsed, washed with a standard shampoo and dried.

The color of the locks was evaluated in the L * a * b * system, on white and permanent hair, using a CM 2002 MINOLTA spectrophotometer. In space L * a * b *, clarity is indicated by the value L * on a scale from 0 to 100 while hue and saturation are expressed by a * and b *: a * and b * indicate two color axes, a * red-green axis and b * yellow-blue axis.

According to this system, the higher the value of L, the lighter and less intense the color. Conversely, the lower the value of L, the darker or very intense the color.

The 4,5-diaminopyrazoles according to the invention therefore make it possible to obtain intense and chromatic shades at alkaline pH.

EXAMPLES 5 AND 6 (Dyes in a neutral environment

The same formulations are produced as above, replacing the ammonia with citric acid in an amount such that the pH is equal to 7.

Gray hair strands containing 90% natural and permanent whites are dyed with the dye compositions 5 and 6 above in the same way as for dyeing at alkaline pH.

The following nuances are obtained:

At neutral pH, the 4,5-diaminoρyrazoles according to the invention make it possible to obtain intense shades.

Claims

1. Diaminopyrazole derivatives of formula

d) in which:

Ri denotes a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, carrying at least one substituent chosen from OR, NHR, NRR ', SR, SOR, SÔ ₂ R, COOH, CONH ₂ , CONRR ', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X denotes H, Na, K or NH ₄ ,

R and R, identical or different, denote a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more functional groups chosen from OH, NH ₂ , OR, NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH ₂ , CONRR', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I , X, R and R 'having the definitions indicated above,

R ₂ denotes H, or a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more functional groups chosen from OH, NH ₂ , Ô | l, NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH ₂ , CONRR', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X, R and R 'having the definitions indicated above, and their physiologically acceptable salts.

2. Compounds of formula (I) according to claim 1 characterized in that the physiologically acceptable salts are acid salts chosen from hydrochlorides, hydrobromides, sulfates, tartrates, lactates or acetates, or salts of bases chosen from soda, potash, ammonia, amines and alkanolamines.

3. Compounds of formula (I) according to claim 1 or 2, characterized in that Ri is a linear Cι-C ₃ alkyl radical, substituted by a group S0 ₃ H, COOH, CONH ₂ , methoxy, 2-hydroxyethyloxy , 2- hydroxyethylamino, mono- or dimethylamino, pyrrolidin-1-yl -3-ol, imidazolidin- 1 -yle, pipérazin- 1 -yle, pipérazin- 1 -y 1-ethanol, tetrahydrofuran-2- yl or tetrahyropyran-2 -yle and R ₂ denote H, methyl, ethyl, 2-hydroxyethyl, 2-methoxyethyl, 2-aminoethyl or carboxymethyl.

4. Compound of formula (I) according to any one of claims 1 to 3, characterized in that it is 4,5-diamino-l- (2'-methoxyethyl) - pyrazole or 4-amino- l- (2'-methoxyethyl) -5-methylaminopyrazole or one of their physiologically acceptable acid salts.

5. Composition for the oxidation dyeing of keratin fibers and in particular human keratin fibers such as the hair, characterized in that it contains, in a medium suitable for dyeing, at least as an oxidation base a 4 , 5-diaminopyrazole of formula (I):

(D in which: Ri denotes a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, carrying at least one substituent chosen from OR, NHR, NRR ', SR, _SOR,. S0 ₂ R, COOH, CONH _2, CONRR ', PO (OH) _2, SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X denotes H, Na, K or NH ₄ , R and R ', identical or different, denote a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more functional groups chosen from OH, NH ₂ , OR, NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH ₂ , CONRR', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X, R and R 'having the definitions indicated above, R ₂ denotes H, or a Cι-C ₆ alkyl or C ₂ -C ₆ alkenyl radical, preferably up to C ₄ , linear or branched, unsubstituted or substituted by one or more functional groups chosen from OH, NH ₂ , OR, NHR, NRR ', SR, SOR, S0 ₂ R, COOH, CONH ₂ , CONRR', PO (OH) ₂ , SH, S0 ₃ X, a non-cationic heterocycle, Cl, Br or I, X, R and R 'having the definitions indicated above, or one of its addition salts with an acid or with a physiologically acceptable base.

6. Composition according to claim 5, characterized in that it contains from 0.001 to 10% by weight of at least one diaminopyrazole of formula (I) or of its salts.

7. Composition according to Claim 6, characterized in that it contains from 0.05 to 6% by weight, and preferably 0.1 to 3% by weight, of at least one diaminopyrazole of formula (I) or of its salts.

8. Composition according to any one of claims 5 to 7, characterized in that the medium suitable for dyeing (or support) consists of water or of a mixture of water and at least one solvent organic chosen from lower alkanols in Cι-C ₄ , polyols and polyol ethers, aromatic alcohols, similar products and their mixtures.

9. Composition according to any one of claims 5 to 8, characterized in that it has a pH of between 3 and 12.

10.Composition according to any one of claims 5 to 9, characterized in that it contains at least one additional oxidation base chosen from paraphenylenediamines, bisphenylalkylenediamines, para-aminophenols, ortho-aminophenols, heterocyclic bases other than diaminopyrazole of formula (I) and their addition salts with an acid.

11. Composition according to Claim 10, characterized in that the additional oxidation base (s) represent from 0.0005 to 12% by weight of the total weight of the dye composition.

12. Composition according to any one of claims 5 to 11, characterized in that it contains at least one coupler and / or at least one direct dye.

13. Composition according to claim 12, characterized in that the coupler or couplers are chosen from metaphenylenediamines, meta- aminophenols, metadiphenols, mono- or polyhydroxylated derivatives of naphthalene and heterocyclic couplers and their addition salts with an acid.

14. Composition according to any one of claims 12 or 13, characterized in that the coupler (s) represent from 0.0001 to 10% by weight of the total weight of the dye composition.

15.Composition according to any one of claims 5 to 14, characterized in that the addition salts with an acid are chosen from hydrochlorides, hydrobromides, sulfates, tartrates, lactates and acetates and salts addition with a base are chosen from those obtained with soda, potash, ammonia or amines.

16. Process for dyeing keratin fibers and in particular human keratin fibers such as the hair, characterized in that at least one dye composition as defined in any one of claims 5 to 16 is applied to these fibers , for a time sufficient to develop the desired coloration, either in air or using an oxidizing agent, optionally in the presence of oxidation catalysts.

17. The method of claim 16, characterized in that the coloring is revealed on contact with air oxygen.

18. The method of claim 16 characterized in that the color is revealed at acidic, neutral or alkaline pH using an oxidizing agent which is added just at the time of use to the dye composition or which is present in an oxidizing composition applied simultaneously or sequentially separately.

19. The method of claim 16 or 18, characterized in that the oxidizing agent is ^' chosen from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulfates.

20 Multi-compartment device, or multi-compartment dyeing "kit", a first compartment of which contains a dye composition as defined in any one of claims 5 to 15 and a second compartment of which contains an oxidizing composition.