WO2003014093A1 - Composition pour la teinture de fibre keratiniques contenant une paraphenylenediamine substituee par un radical diazacycloheptane - Google Patents
Composition pour la teinture de fibre keratiniques contenant une paraphenylenediamine substituee par un radical diazacycloheptane Download PDFInfo
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- WO2003014093A1 WO2003014093A1 PCT/FR2002/002822 FR0202822W WO03014093A1 WO 2003014093 A1 WO2003014093 A1 WO 2003014093A1 FR 0202822 W FR0202822 W FR 0202822W WO 03014093 A1 WO03014093 A1 WO 03014093A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D243/00—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms
- C07D243/06—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4
- C07D243/08—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1 and 4 not condensed with other rings
Definitions
- the subject of the invention is a composition for the oxidation dyeing of keratin fibers, in particular human hair, comprising an oxidation base of the paraphenylenediamine type substituted with a diazacycloheptane radical.
- the invention also relates to the process for dyeing fibers using this composition, as well as the new compounds of the type mentioned above. It is known to dye keratin fibers and in particular human hair with dye compositions containing oxidation dye precursors, generally called oxidation bases, such as ortho or paraphenylenediamines, ortho or paraaminophenols and heterocyclic compounds. These oxidation bases are colorless or weakly colored compounds which, associated with oxidizing products, can give rise, through an oxidative condensation process, to colored compounds.
- couplers are chosen in particular from aromatic metadiamines, metaaminophenols, metadiphenols and certain heterocyclic compounds. such as indole compounds.
- the object of the present invention is to provide new compositions for dyeing keratin fibers which do not have the drawbacks of those of the prior art.
- the aim of the present invention is to provide compositions which have powerful, not very selective and particularly resistant dyes, while being capable of generating intense colorings in various shades, in particular in the fundamental shades.
- composition for the oxidation dyeing of keratin fibers comprising an oxidation base of formula (I) below and / or the corresponding addition salts:
- Ri represents - a halogen atom, preferably chlorine or bromine
- - a hydrocarbon chain of CrC 6 , saturated or which may contain one or more double bonds and / or one or more triple bonds, linear or branched, which may form a ring having 3 to 6 members, one or more carbon atoms which may be replaced by an oxygen, nitrogen or sulfur atom, by an SO 2 group, or when the carbon is terminated by a halogen atom, preferably an atom chlorine or bromine; said radical R not comprising a peroxide bond, nor of diazo, nitro or nitroso radicals;
- n is between 0 and 4 inclusive, it being understood that when n is greater than or equal to 2 then the radicals Rj can be identical or different, • R 2 represents
- alkyl radical which may be unsaturated, unsubstituted or substituted by one or more carboxylic, alkylcarbonyl, alkoxycarbonyl, carbamoyl, mono- or di-alkylcarbamoyl, heterocyclic nitrogen, oxygenated and / or sulfur, saturated and / or unsaturated radicals at 4, 5 , 6 or 7 atoms;
- alkyl radical which may be unsaturated, substituted in position 2 or more by one or more hydroxy, alkoxy, amino, mono- or di-alkylamino, thiol or halogen radicals;
- R 6 R 7 NC NR 5 - where R 5 , R 6 and R 7 represent a hydrogen, a CC 4 alkyl radical or a hydroxyalkyl radical, preferably R 5 is hydrogen and R 6 and R are chosen from hydrogen or methyl, • R 3 represents
- an aminoalkyl radical the amine possibly being mono or disubstituted by an alkyl, acetyl or hydroxyalkyl radical;
- an aminoalkyl radical the amine possibly being mono or disubstituted by an alkyl, acetyl, hydroxyalkyl radical; - a hydroxy- and aminoalkyl radical;
- m is between 0 and 4 inclusive, it being understood that when m is greater than or equal to 2 then the radicals R 4 may be identical or different.
- the compounds of formula (I) are paraphenylene diamines substituted by a substituent of type 1, 4-diazacycloheptane, a substituent also called in the literature 1, 4-diazepane.
- radicals or alkyl groups are linear or branched and comprise, unless otherwise indicated, from 1 to 10 carbon atoms, preferably 1 to 6 carbon atoms.
- An alkoxy radical is an alkyl-O radical, the alkyl group being as defined above.
- An unsaturated alkyl radical is understood to mean an alkyl of 2 to 10 carbon atoms and comprising one or more double and / or triple bonds.
- a substituted alkyl radical is a mono or polysubstituted alkyl.
- a hydroxyalkyl or aminoalkyl is an alkyl which may be substituted by one or more hydroxy or amino groups.
- An alkyl radical substituted in position 2 or more is an alkyl of formula -CH 2 -R, R being a substituted alkyl.
- radical Ri when it is indicated that one or more of the carbon atoms of the radical Ri can be replaced by an oxygen, nitrogen, or sulfur atom or by an SO 2 group, and / or that said radical Ri can contain one or more double bonds and / or one or more triple bonds, this means that the following transformations can be made, for example:
- the benzene ring is NH 2 -C 6 H 4 -N-.
- the radical Ri is for example chosen from a chlorine atom, a methyl, ethyl, isopropyl, vinyl, allyl, methoxymethyl, hydroxymethyl, 1 -carboxymethyl, 1-aminomethyl radical , 2-carboxyethyl, 2-hydroxyethyl, 3-hydroxypropyl, 1, 2-dihydroxyethyl, 1-hydroxy-2 aminoethyl, 1-amino-2-hydroxy ethyl, 1, 2-diaminoethyl, methoxy, ethoxy, allyloxy, 2- hydroxyethyloxy.
- R 1 is preferably an alkyl, hydroxyalkyl or aminoalkyl, alkoxy, hydroxyalkoxy radical.
- Ri can be chosen from a methyl, hydroxymethyl, 2-hydroxyethyl, 1,2-dihydroxyethyl, methoxy, 2-hydroxyethoxy radical and more preferably, a methyl radical, a hydroxymethyl radical or a 1,2-dihydroxyethyl radical.
- the oxidation bases of formula (I) are such that n is equal to 0 or 1.
- the radical R 2 is chosen from hydrogen, an alkyl radical, an alkyl radical substituted by a heterocyclic nitrogenous, oxygenated and / or sulfur, saturated or unsaturated, at 4.5, 6 or 7 atoms, an alkoxycarbonyl radical, an alkyl radical substituted in position 2 or more by one or more hydroxy radicals.
- R 2 can be chosen from the 2-hydroxyethyl radical, the 3 (1-pyrrolidinyl) propyl radical, the methyl radical, the acetyl radical, hydrogen, and more preferably the 2-hydroxyethyl radical, the methyl or hydrogen radical.
- R 3 is chosen from hydrogen, an alkyl radical, an alkyl radical substituted by one or more hydroxy, an alkyl radical substituted by one or more amino, a carboxyl radical.
- R 3 can be chosen from hydrogen, the hydroxyl radical, the carboxyl radical, the amino radical, the hydroxymethyl radical, the aminomethyl radical.
- R 3 more preferably represents a hydrogen radical.
- R 4 is chosen from hydrogen, an alkyl radical, an alkyl radical substituted by one or more hydroxy, an alkyl radical substituted by one or more amino, a carboxyl radical.
- R 4 preferably represents hydrogen.
- the carbon substituted by R 3 or by R 4 can be of configuration (R) and / or (S).
- the addition salts corresponding to formula (I) may be addition salts with an acid or addition salts with a base.
- the oxidation bases of formula (I) are chosen from the following compounds or their addition salts with an acid or a base
- the oxidation base (s) of formula (I) are generally present in an amount of between 0.001 and 10% by weight approximately of the total weight of the dye composition and preferably between 0.005 and 6%.
- composition of the present invention may further comprise one or more additional oxidation bases.
- additional oxidation bases are chosen from the oxidation bases conventionally used in oxidation dyeing, for example paraphenylenediamines, bis-phenylalkylenediamines, para-aminophenols, ortho-aminophenols and heterocyclic bases and their salts. addition.
- paraphenylenediamines there may be mentioned by way of example, 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- ( ⁇ - hydroxyethyl) paraphenylenediamine, 4-N, N-bis- ( ⁇ -hydroxyethyl) amino 2- methyl aniline, 4-N, N-bis- ( ⁇ -hydroxyethyl) amino 2-chloro aniline, 2- ⁇ -hydroxyethyl parapheny
- paraphenylenediamine paratoluylenediamine, 2-isopropyl paraphenylenediamine, 2- ⁇ -hydroxyethyl paraphenylenediamine, 2- ⁇ -hydroxyethyloxy paraphenylenediamine, 2,6-dimethyl paraphenylenediamine paraphenylenediamine, 2,3-dimethyl paraphenylenediamine, N, N-bis- ( ⁇ -hydroxyethyl) paraphenylenediamine, 2-chloro paraphenylenediamine, 2- ⁇ -acetylaminoethyloxy paraphenylenediamine, and their addition salts with an acid are particularly preferred .
- bis-phenylalkylenediamines that may be mentioned by way of example,
- para-aminophenol there may be mentioned by way of example, 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- ( ⁇ -hydroxyethyl aminomethyl) phenol, 4- amino 2-fluoro phenol, and their addition salts with an acid.
- 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- ( ⁇ -hydroxyethyl aminomethyl) phenol, 4- amino 2-fluoro phenol, and their addition salts with an acid.
- ortho-aminophenols there may be mentioned 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.
- heterocyclic bases for example, pyridine derivatives, pyrimidine derivatives and pyrazole derivatives.
- pyridine derivatives mention may be made 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- ( ⁇ -methoxyethyl) amino 3-amino 6-methoxy pyridine, 3,4-diamino pyridine, and their addition salts with an acid.
- pyrimidine derivatives mention may be made of the compounds described for example in patents DE 2 359399; JP 88-169571; 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
- the additional oxidation bases are generally present in an amount between 0.001 to 10% by weight approximately of the total weight of the dye composition, and preferably from 0.005 to 6%.
- the composition according to the invention may contain one or more couplers conventionally used for dyeing keratin fibers.
- couplers conventionally used for dyeing keratin fibers.
- couplers mention may in particular be made of metaphenylenediamines, meta-aminophenols, metadiphenols, naphthalene couplers and heterocyclic couplers and their addition salts.
- the addition salts with an acid which can be used in the context of the dye compositions of the invention for the oxidation bases of formula (I), the additional oxidation bases and the couplers are in particular chosen from hydrochlorides, hydrobromides, sulfates, citrates, succinates, tartrates, lactates, tosylates, benzenesulfonates, phosphates and acetates.
- addition salts with a base which can be used in the context of the invention are for example chosen from addition salts with soda, potassium hydroxide, ammonia, amines or alkanolamines.
- 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, azo direct dyes, methinic direct dyes.
- the medium suitable for dyeing also called dye support, generally consists of water or of a mixture of water and at least one organic solvent to dissolve the compounds which are not sufficiently soluble in water.
- organic solvent mention may, for example, be made of lower CrC alkanols, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, monoethyl ether and diethylene glycol monomethyl ether, as well as aromatic alcohols such as benzyl alcohol or phenoxyethanol, and mixtures thereof.
- 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 dye composition in accordance with the invention may also contain various adjuvants conventionally used in compositions for dyeing hair, such as anionic, cationic, nonionic, amphoteric, zwitteronic surfactants or mixtures thereof, anionic, cationic, nonionic, amphoteric, zwitterionic polymers or mixtures thereof, inorganic or organic thickeners, and in particular associative thickeners, anionic, cationic, nonionic and amphoteric polymers, antioxidants, penetration agents, sequestering agents, perfumes, buffers, dispersing agents, conditioning agents such as, for example, volatile or non-volatile silicones volatile, modified or unmodified, film-forming agents, ceramides, preserving agents, opacifying agents.
- adjuvants are generally present in an amount for each of them of between 0.01 and 20% by weight relative to the weight of the composition.
- 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 keratin fibers or even using conventional buffer systems.
- 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.
- 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.
- 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:
- 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 invention also relates to a process for dyeing keratin fibers and in particular human keratin fibers such as the hair, using the composition of the invention.
- the composition according to the present invention 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 to the composition of the invention just at the time of use or it can be used from an oxidizing composition containing it , applied simultaneously or sequentially to the composition of the invention.
- the composition according to the present invention is mixed, preferably at the time of use, with a composition containing, in a medium suitable for dyeing, at least one oxidizing agent, this oxidizing agent being present in enough to develop color.
- 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 agents conventionally used for the oxidation dyeing of keratin fibers are for example hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulfates, peracids and enzymes oxidases among which there may be mentioned peroxidases, 2-electron oxidoreductases such as uricases and 4-electron oxygenases such as laccases. Hydrogen peroxide is particularly preferred.
- the oxidizing composition may also contain various adjuvants conventionally used in compositions for dyeing the hair and as defined above for the composition of the invention.
- 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 varies between 3 and 12 approximately, and preferably between 5 and 11. It can be adjusted to the desired value by means of acidifying or basifying agents usually used in dyeing keratin fibers and as defined above.
- 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 composition for the dye 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 also the colored product capable of being obtained by oxidative condensation of the composition of the present invention.
- This composition comprises at least one oxidation base of formula (I) as defined above in the presence of at least one oxidizing agent as defined above and optionally in the presence of at least one coupler and / or at least an additional oxidation base.
- These colored products may in particular be in the form of pigments and be used as direct dye for the direct dyeing of the hair or even be incorporated in cosmetic products such as for example in makeup products.
- the present invention finally relates to the new paraphenylenediamine derivatives of formula (I) with the exception of 4- (4-methyl- [1, 4] diazepan-1-yl) - phenylamine.
- the examples which follow serve to illustrate the invention without, however, being limiting in nature.
- Step 2 synthesis of 4-.4-Methyl-ri.41diazepan-1-vh-phenylamine.
- dichlorhvdrate (2) In a stainless steel hydrogenating reactor, 6 g of 1-methyl-4- (4-nitro-phenyl) - [1, 4] diazepane (1) (25.5 mmol) are partially dissolved in 300 ml of ethanol. 2.1 g of 5% Pd / C (50% wet) are added, the reactor is closed and purged with nitrogen 3 times with stirring (1800 rpm). The hydrogen is then introduced under a pressure of 12 bar at room temperature for 4 hours.
- Step 1 Synthesis of 1 - (3-Methyl-4-nitro-phenvfl- ⁇ .41diazepane M): The fluoronitrobenzene (9.1 g, 0.0586 mol.) Is dissolved in water (50 ml) and then potassium carbonate (9.7 g, 0.0703 mol.) And 1-acetyl are added. ) - [1, 4] diazepane (10 g, 0.0703 mol.). The mixture is heated at 95 ° C. for 6 hours, an orange solution is obtained. Then cooled to room temperature, there is then an orange sticky paste. The maximum amount of water is removed from the reaction medium. Then isopropanol is added to the paste until precipitation of a yellow solid.
- Step 2 synthesis of 1 - (3-Methyl-4-nitro-phenvh-f 1.41diazepane (2):
- Step 3 Synthesis of 4- ⁇ .4lDiazepan-1-yl-2-methyl-phenylamine.
- dichlorhvdrate (3) 2.34 g of 1 - (3-methyl-4-nitro-phenyl) - [1, 4] diazepane 2 (9.96 mmol) are dissolved in 150 ml in a stainless steel hydrogenating reactor ethanol. 1.2 g of 5% Pd / C (50% wet) are added, the reactor is closed and purged with nitrogen 3 times with stirring (1800 rpm). The hydrogen is then introduced under a pressure of 9 bars at room temperature for 3 hours.
- Eta p s 1 s y n ceremonies du1- (4-Nitro- p hényl) -4- (3-p yrrolidin-1-yl-p ro py lH1.41diazepane):
- Step 2 synthesis of, 4-f4- (3-Pyrrolidin-1-yl-propylH1.41diazepan-1-v ⁇ -phenylamine.
- Step 1 Synthesis of 1 -Benzyl-4-, 4-nitro-phenylH 1, 41diazepane (11: Fluoronitrobenzene (3.09 g, 21.9 mmol) is placed in water (14 ml), then potassium carbonate (3.64 g, 26.28 mmol) and 1-benzyl homopiperazine (5) are added. g, 26.28 mmol). It is heated to 90 ° C. for 4.20 hrs and then cooled to room temperature. The precipitate formed is filtered, a yellow solid is obtained. 6.30 g (92.5%) of product are recovered.
- the reactor is then purged with nitrogen and the reaction medium is filtered under a nitrogen atmosphere and the filtrate is immediately recovered in a solution containing 7.6 ml of 37% hydrochloric acid and 30 ml of isopropanol.
- the filtrate is then concentrated until a precipitate is obtained.
- the solid is filtered, washed with isopropanol and then dried under vacuum in the presence of potassium hydroxide. 4.6 g of 4- [1, 4] Diazepan-1-yl-phenylamine, dihydrochloride (2) are thus obtained in the form of a white solid.
- compositions were prepared (content of bases and couplers in mole)
- each composition is mixed with an equal weight of hydrogen peroxide at 20 volumes (6% by weight).
- Each mixture obtained is applied to locks of gray hair containing 90% natural or permanent whites. After 30 min of laying, the locks are rinsed, washed with a standard shampoo, rinsed again and then dried.
- the color of the locks was evaluated in the L * a * b * system , using a CM 2002 MINOLTA spectrophotometer.
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Abstract
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Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US10/485,855 US7241317B2 (en) | 2001-08-08 | 2002-08-07 | Composition for dyeing keratin fibers comprising at least one para-phenylenediamine substituted with a diazacycloheptane radical |
DE60222141T DE60222141T2 (de) | 2001-08-08 | 2002-08-07 | Zusammensetzung zum Färben von Keratinfasern, die ein mit einer Diazacycloheptangruppe substituiertes p-Phenylendiamin enthält |
EP02772490A EP1417184B1 (fr) | 2001-08-08 | 2002-08-07 | Composition pour la teinture de fibre keratiniques contenant une paraphenylenediamine substituee par un radical diazacycloheptane |
JP2003519043A JP2005504046A (ja) | 2001-08-08 | 2002-08-07 | ジアザシクロヘプタン基で置換されたパラフェニレンジアミンを含有するケラチン繊維を染色するための組成物 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR01/10597 | 2001-08-08 | ||
FR0110597A FR2828488B1 (fr) | 2001-08-08 | 2001-08-08 | Composition pour la teinture de fibres keratiniques contenant une paraphenylenediamine substituee par un radical diazacycloheptane |
Publications (1)
Publication Number | Publication Date |
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WO2003014093A1 true WO2003014093A1 (fr) | 2003-02-20 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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PCT/FR2002/002822 WO2003014093A1 (fr) | 2001-08-08 | 2002-08-07 | Composition pour la teinture de fibre keratiniques contenant une paraphenylenediamine substituee par un radical diazacycloheptane |
Country Status (9)
Country | Link |
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US (1) | US7241317B2 (fr) |
EP (1) | EP1417184B1 (fr) |
JP (1) | JP2005504046A (fr) |
AR (1) | AR034983A1 (fr) |
AT (1) | ATE371651T1 (fr) |
DE (1) | DE60222141T2 (fr) |
ES (1) | ES2292813T3 (fr) |
FR (1) | FR2828488B1 (fr) |
WO (1) | WO2003014093A1 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1462445A1 (fr) * | 2003-03-24 | 2004-09-29 | L'oreal | Dérivés de paraphénylènediamine à groupement cyclique diaza substitué par un radical cationique et utilisation de ces dérivés pour la coloration de fibres kératiniques |
US7090703B2 (en) | 2003-03-24 | 2006-08-15 | L'oreal | Para-phenylenediamine derivatives comprising a cyclic diaza group substituted with a cationic radical, and use of these derivatives for dyeing keratin fibers |
US7186277B2 (en) | 2003-03-24 | 2007-03-06 | L'oreal Sa | Composition for dyeing keratin fibres, comprising a cationic para-phenylenediamine derivative substituted with a diazacyclohexane or diazacycloheptane ring |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2852830B1 (fr) * | 2003-03-24 | 2008-04-18 | Oreal | Composition de teinture des fibres keratiniques comprenant un derive de para-phenylenediamine cationique substitue par un cycle diazacyclohexane ou diazacycloheptane |
FR2856059B1 (fr) * | 2003-06-13 | 2005-10-28 | Oreal | Derives de para-phenylenediamine comportant un cycle diazacycloheptane substitue par un radical silyle pour la teinture des fibres keratiniques |
FR2860232B1 (fr) * | 2003-09-26 | 2006-01-27 | Oreal | Derives de triacyclonane substitue sur l'un au moins des atomes d'azote par un groupement 4'-aminophenyle substitue ou non substitue pour la teinture des fibres keratiniques |
DE102006018345A1 (de) * | 2006-04-19 | 2007-10-25 | Henkel Kgaa | Aufhell- und/oder Färbemittel mit Amidinen |
EP2047841B1 (fr) * | 2006-07-31 | 2016-10-26 | Kao Corporation | Composition de coloration des cheveux |
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FR2733749B1 (fr) | 1995-05-05 | 1997-06-13 | Oreal | Compositions pour la teinture des fibres keratiniques contenant des diamino pyrazoles, procede de teinture, nouveaux diamino pyrazoles et leur procede de preparation |
DE19539264C2 (de) | 1995-10-21 | 1998-04-09 | Goldwell Gmbh | Haarfärbemittel |
DE19543988A1 (de) | 1995-11-25 | 1997-05-28 | Wella Ag | Oxidationshaarfärbemittel mit einem Gehalt an 3,4,5-Triaminopyrazolderivaten sowie neue 3,4,5-Triaminopyrazolderivate |
FR2750048B1 (fr) | 1996-06-21 | 1998-08-14 | Oreal | Compositions de teinture des fibres keratiniques contenant des derives pyrazolo-(1, 5-a)-pyrimidine, procede de teinture, nouveaux derives pyrazolo-(1, 5-a)-pyrimidine et leur procede de preparation |
WO2000047558A1 (fr) * | 1999-02-10 | 2000-08-17 | Welfide Corporation | Composes amide et leur utilisation medicinale |
-
2001
- 2001-08-08 FR FR0110597A patent/FR2828488B1/fr not_active Expired - Fee Related
-
2002
- 2002-08-07 DE DE60222141T patent/DE60222141T2/de not_active Expired - Lifetime
- 2002-08-07 WO PCT/FR2002/002822 patent/WO2003014093A1/fr active IP Right Grant
- 2002-08-07 EP EP02772490A patent/EP1417184B1/fr not_active Expired - Lifetime
- 2002-08-07 AR ARP020102982A patent/AR034983A1/es not_active Application Discontinuation
- 2002-08-07 AT AT02772490T patent/ATE371651T1/de not_active IP Right Cessation
- 2002-08-07 ES ES02772490T patent/ES2292813T3/es not_active Expired - Lifetime
- 2002-08-07 JP JP2003519043A patent/JP2005504046A/ja active Pending
- 2002-08-07 US US10/485,855 patent/US7241317B2/en not_active Expired - Fee Related
Patent Citations (5)
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WO1998038175A1 (fr) * | 1997-02-26 | 1998-09-03 | Henkel Kommanditgesellschaft Auf Aktien | Nouveaux derives de 1,4-diazacycloheptane et leur utilisation dans des colorants capillaires d'oxydation |
WO1998058926A1 (fr) * | 1997-06-20 | 1998-12-30 | Celltech Therapeutics Limited | Derives de 2-aminopyrimidine polycycliques condensees inhibiteurs de la proteine kinase |
JPH11139969A (ja) * | 1997-08-07 | 1999-05-25 | Tanabe Seiyaku Co Ltd | 医薬組成物 |
EP0962452A1 (fr) * | 1998-05-13 | 1999-12-08 | Bristol-Myers Squibb Company | Composition de teinture d'oxydation et procédés comprenant de dérivés 2-pyrrolidineméthanol 1-(4-aminophényle) |
WO2002006278A1 (fr) * | 2000-07-17 | 2002-01-24 | Ranbaxy Laboratories Limited | Derives d'oxazolidinone utilises en tant qu'antimicrobiens |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1462445A1 (fr) * | 2003-03-24 | 2004-09-29 | L'oreal | Dérivés de paraphénylènediamine à groupement cyclique diaza substitué par un radical cationique et utilisation de ces dérivés pour la coloration de fibres kératiniques |
FR2852955A1 (fr) * | 2003-03-24 | 2004-10-01 | Oreal | Derives de paraphenylenediamine a groupement cyclique diaza substitue par un radical cationique et utilisation de ces derives pour la coloration de fibres keratiniques |
US7090703B2 (en) | 2003-03-24 | 2006-08-15 | L'oreal | Para-phenylenediamine derivatives comprising a cyclic diaza group substituted with a cationic radical, and use of these derivatives for dyeing keratin fibers |
US7186277B2 (en) | 2003-03-24 | 2007-03-06 | L'oreal Sa | Composition for dyeing keratin fibres, comprising a cationic para-phenylenediamine derivative substituted with a diazacyclohexane or diazacycloheptane ring |
Also Published As
Publication number | Publication date |
---|---|
FR2828488A1 (fr) | 2003-02-14 |
DE60222141D1 (de) | 2007-10-11 |
JP2005504046A (ja) | 2005-02-10 |
US7241317B2 (en) | 2007-07-10 |
DE60222141T2 (de) | 2008-06-05 |
AR034983A1 (es) | 2004-03-24 |
EP1417184A1 (fr) | 2004-05-12 |
US20050102769A1 (en) | 2005-05-19 |
ES2292813T3 (es) | 2008-03-16 |
FR2828488B1 (fr) | 2005-06-10 |
EP1417184B1 (fr) | 2007-08-29 |
ATE371651T1 (de) | 2007-09-15 |
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