Patent Grant
6946005
The disclosure relates to novel pyrrolidinyl-substituted para-phenylenediamine derivatives comprising a cationic radical chosen from compounds of formula (I), as defined herein. This disclosure also relates to the dye compositions comprising them and the process for dyeing keratin fibers using these compositions.
It is well-known practice to dye keratin fibers, such as human hair, with dye compositions comprising oxidation dye precursors, also known as oxidation bases, such as ortho- or para-phenylenediamines, ortho- or para-aminophenols, heterocyclic compounds such as diaminopyrazole derivatives, pyrazolo[1,5-a]pyrimidine derivatives, pyrimidine derivatives, pyridine derivatives, 5,6-dihydroxyindole derivatives and 5,6-dihydroxyindoline derivatives. Oxidation dye precursors, or oxidation bases, are colorless or weakly colored compounds that, when combined with oxidizing products, can give rise to colored compounds and dyes by a process of oxidative condensation.
It is also known that the shades obtained with these oxidation bases may be varied by combining them with couplers or coloration modifiers. These couplers or coloration modifiers may be chosen, for example, from aromatic meta-diamines, meta-aminophenols, meta-hydroxyphenols and certain heterocyclic compounds such as, for example, pyrazolo[1,5-b]-1,2,4-triazole derivatives, pyrazolo[3,2-c]-1,2,4-triazole derivatives, pyrazolo[1,5-a]pyrimidine derivatives, pyridine derivatives, pyrazol-5-one derivatives, indoline derivatives and indole derivatives.
The variety of molecules used as oxidation bases and couplers make it possible to obtain a wide range of colors.
The “permanent” coloration obtained with these oxidation dyes should moreover satisfy a number of requirements. For example, it should have no toxicological drawbacks, it should allow shades to be obtained in the desired intensity, and it should show good resistance to external agents such as light, bad weather, washing, permanent-waving, perspiration and rubbing.
The oxidation dyes should also, for example, allow white hairs to be covered. Further, the oxidation dyes should be as unselective as possible, i.e., they should produce the smallest possible color differences along the same length of keratin fiber, which may be differently sensitized (i.e. damaged) between its end and its root. The oxidation dyes should also, for example, show good chemical stability in the formulations, and, further for example, have a good toxicological profile.
In the field of hair dyeing, para-phenylenediamine and para-tolylenediamine are oxidation bases that are widely used. These oxidation bases may, for example, provide varied shades when used with oxidation couplers.
However, there is a need to discover novel oxidation bases that may have a better toxicological profile than para-phenylenediamine and para-tolylenediamine, while at the same time may give the hair at least one of the following excellent properties: color intensity, variety of shades, color uniformity and fastness with respect to external agents.
It is already known practice to use para-phenylenediamine derivatives substituted with a pyrrolidine group as oxidation bases for dyeing keratin fibers. For example, U.S. Pat. No. 5,851,237 discloses the use of 1-(4-aminophenyl)pyrrolidine derivatives optionally substituted on the benzene nucleus, to replace para-phenylenediamine.
U.S. Pat. No. 5,993,491 discloses the use of N-(4-aminophenyl)-2-hydroxymethylpyrrolidine derivatives optionally substituted on the benzene nucleus and on the pyrrolidine heterocycle in position 4 with a hydroxyl radical, in order to replace para-phenylenediamine.
Japanese Patent Application 11-158 048 discloses compositions containing at least one compound chosen from 4-aminoaniline derivatives optionally substituted on the benzene nucleus, and one of the nitrogen atoms of which is included in a 5- to 7-membered carbon ring.
It is established that these compounds may not make it possible to give the hair a coloration that is equivalent in quality to that obtained with para-phenylenediamine or with para-tolylenediamine due to the lack of intensity and color uniformity.
There is thus a real need to discover novel oxidation bases that may, for example, have both a good toxicological profile and properties such that the compositions comprising them may be able to give the hair at least one of the following excellent properties: color intensity, variety of shades, color uniformity and fastness with respect to the various attacking factors to which the hair may be subjected.
Disclosed herein are novel dye compositions that can overcome at least one drawback of the oxidation bases of the prior art. For example, disclosed herein are novel dye compositions for dyeing keratin fibers, which do not degrade the keratin fibers, while at the same time are capable of generating intense colorations in varied shades, and which may be unselective, resistant and can have a good toxicological profile.
Further disclosed herein is a compound chosen from pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and the addition salts thereof
wherein
For example, R1 may be chosen from a chlorine atom, and methyl, ethyl, isopropyl, vinyl, allyl, methoxymethyl, hydroxyethyl, 1-carboxymethyl, 1-aminomethyl, 2-carboxyethyl, 2-hydroxyethyl, 3-hydroxypropyl, 1,2-dihydroxyethyl, 1-hydroxy-2-aminoethyl, 1-amino-2-hydroxyethyl, 1,2-diaminoethyl, methoxy, ethoxy, allyloxy and 2-hydroxyethyloxy radicals.
Further disclosed herein is a dyeing composition comprising, in a medium suitable for dyeing keratin fibers, at least one oxidation base chosen from pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and the addition salts thereof.
Also disclosed herein is the use of this composition for dyeing keratin fibers and the process for dyeing keratin fibers, for example, human keratin fibers such as hair, using the composition disclosed herein.
The composition disclosed herein may make it possible to obtain, for example, a chromatic, powerful, unselective and fast coloration of keratin fibers.
As used herein, an aliphatic hydrocarbon-based chain is chosen from linear and branched chains that may comprise at least one unsaturation chosen from unsaturations of the alkene type and the alkyne type. An alicyclic hydrocarbon-based chain is chosen from saturated and unsaturated, linear and branched chains not containing an aromatic cyclic structure.
When the aliphatic hydrocarbon-based chain or the alicyclic hydrocarbon-based chain is interrupted with an entity Y chosen from an oxygen atom, a sulphur atom, a nitrogen atom, a silicon atom and a SO2 radical, a unit CH2—Y—CH2 is obtained, for example.
The term “onium” means a nitrogen-based quaternary radical.
In formula (I), when n is equal to 1, R1 may, for example, be chosen from halogen atoms; C1-C6 aliphatic and alicyclic, saturated and unsaturated hydrocarbon-based chains, at least one carbon atom possibly being replaced with an entity chosen from an oxygen atom, a nitrogen atom, a silicon atom, a sulphur atom, and a SO2 radical, with the proviso that the radical R1 does not comprise a peroxide bond, a diazo radical, a nitro radical or a nitroso radical. R1 may also, for example, be chosen from chlorine, bromine and C1-C4 alkyl, C1-C4 hydroxyalkyl, C1-C4 aminoalkyl, C1-C4 alkoxy and C1-C4 hydroxyalkoxy radicals. Further, for example, R1 may be chosen from methyl, hydroxymethyl, 2-hydroxyethyl, 1,2-dihydroxyethyl, methoxy, isopropyloxy and 2-hydroxyethoxy radicals.
The onium radicals Z may be chosen from radicals of formula (II)
wherein
In formula (II), when x is equal to 0, then R4, R5 and R6, which may be identical or different, are each, for example, chosen from C1-C6 alkyl radicals, C1-C4 monohydroxyalkyl radicals, C2-C4 polyhydroxyalkyl radicals, (C1-C6)alkoxy(C1-C4)alkyl radicals, C1-C6 amidoalkyl radicals, tri(C1-C6)alkylsilane(C1-C6)alkyl radicals, or R4 and R5 form, together with the nitrogen to which they are attached, a ring chosen from azetidine, pyrrolidine, piperidine, piperazine and morpholine rings, R6 being chosen in this case from C1-C6 alkyl radicals; C1-C6 monohydroxyalkyl radicals; C2-C6 polyhydroxyalkyl radicals; C1-C6 aminoalkyl radicals; C1-C6 aminoalkyl radicals wherein the amine may be mono- or disubstituted with a radical or two radicals, chosen from (C1-C6)alkyl, (C1-C6)alkylcarbonyl, amido and (C1-C6)alkylsulphonyl radicals; C1-C6 carbamylalkyl radicals; tri(C1-C6)alkylsilane(C1-C6)alkly radicals; (C1-C6)alkylcarboxy(C1-C6)alkyl radicals; (C1-C6)alkylcarbonyl(C1-C6)alkyl radicals; and N-(C1-C6)alkylcarbamyl(C1-C6)alkyl radicals.
When x is equal to 1, then R7 is, for example, chosen from C1-C6 alkyl radicals; C1-C6 monohydroxyalkyl radicals; C2-C6 polyhydroxyalkyl radicals; C1-C6 aminoalkyl radicals; C1-C6 aminoalkyl radicals wherein the amine may be mono- or disubstituted with a radical or two radicals, which may be identical or different, chosen from (C1-C6)alkyl, (C1-C6)alkylcarbonyl, amido and (C1-C6)alkylsulphonyl radicals; C1-C6 carbamylalkyl radicals; tri(C1-C6)alkylsilane(C1-C6)alkyl radicals; (C1-C6)alkylcarboxy-(C1-C6)alkyl radicals; (C1-C6)alkylcarbonyl(C1-C6)alkyl radicals; and N-(C1-C6)alkylcarbamyl(C1-C6)alkyl radicals; R4 and R5 form, together with the nitrogen to which they are attached, a ring chosen from azetidine, pyrrolidine, piperidine, piperazine and morpholine rings, R6 being chosen in this case from C1-C6 alkyl radicals; C1-C6 monohydroxyalkyl radicals; C2-C6 polyhydroxyalkyl radicals; C1-C6 aminoalkyl radicals; C1-C6 aminoalkyl radicals wherein the amine may be mono- or disubstituted with a radical or two radicals, which may be identical or different, chosen from (C1-C6)alkyl, (C1-C6)alkylcarbonyl, amido and (C1-C6)alkylsulphonyl radicals; C1-C6 carbamylalkyl radicals; tri(C1-C6)alkylsilane(C1-C6)alkyl radicals; (C1-C6)alkylcarboxy(C1-C6)alkyl radicals; (C1-C6)alkylcarbonyl(C1-C6)alkyl radicals; and N-(C1-C6)alkylcarbamyl(C1-C6)alkyl radicals.
In formula (II), the linking arm D may, for example, be chosen from a covalent bond and an alkylene chain that may be substituted.
The onium radicals Z may be chosen from radicals of formula (III)
wherein
By way of example, the ring members E, G, J and L, together with the ring nitrogen, may form a ring chosen from pyrrole, imidazole, pyrazole, oxazole, thiazole and triazole rings. In one embodiment, the ring members E, G, J and L, together with the ring nitrogen, form an imidazole ring.
In another embodiment, the onium radicals Z are chosen from radicals of formula (III), wherein x is equal to 0 and the linking arm D is chosen from a covalent bond and an alkylene chain that may be substituted.
The onium radicals Z may be chosen from radicals of formula (IV)
wherein:
In one embodiment, the ring members E, G, J, L and M form, with the nitrogen of the ring, a ring chosen from pyridine and pyrimidine rings.
When x is equal to 0, then R is chosen, for example, from a hydroxyl radical, C1-C6 alkyl radicals, C1-C6 monohydroxyalkyl radicals, C2-C6 polyhydroxyalkyl radicals, C1-C6 alkoxy radicals, tri(C1-C6)alkylsilane(C1-C6)alkyl radicals, amido radicals, C1-C6 alkylcarbonyl radicals, amino radicals, amino radicals mono- or disubstituted with a radical or two radicals, which may be identical or different, chosen from (C1-C6)alkyl, (C1-C6)alkylcarbonyl, amido and (C1-C6)alkylsulphonyl radicals; C1-C6 monohydroxyalkyl radicals and C2-C6 polyhydroxyalkyl radicals, and R3 is chosen from C1-C6 alkyl radicals, C1-C6 monohydroxyalkyl radicals, C2-C6 polyhydroxyalkyl radicals, tri(C1-C6)alkylsilane(C1-C6)alkyl radicals, (C1-C6)alkoxy(C1-C6)alkyl radicals and C1-C6 carbamylalkyl radicals.
When x is equal to 1, R7 is chosen, for example, from C1-C6 alkyl radicals; C1-C6 monohydroxyalkyl radicals; C2-C6 polyhydroxyalkyl radicals; C1-C6 aminoalkyl radicals; C1-C6 aminoalkyl radicals wherein the amine is mono- or disubstituted with a radical or two radicals, which may be identical or different, chosen from (C1-C6)alkyl radicals, (C1-C6)alkylcarbonyl radicals, amido radicals and (C1-C6)alkylsulphonyl radicals; C1-C6 carbamylalkyl radicals; tri(C1-C6)alkylsilane(C1-C6)alkyl radicals; (C1-C6)alkylcarbony(C1-C6)alkyl radicals; and N-(C1-C6)alkylcarbamyl(C1-C6)alkyl radicals; R is chosen from a hydroxyl radical, C1-C6 alkyl radicals, C1-C6 monohydroxyalkyl radicals, C2-C6 polyhydroxyaklyl radicals, C1-C6 alkoxy radicals, tri(C1-C6)alkylsilane(C1-C6)alkyl radicals, amido radicals, C1-C6 alkylcarbonyl radicals, amino radicals, amino radicals mono- or disubstituted with a radical or two radicals, which may be identical or different, chosen from (C1-C6)alkyl, (C1-C6)alkylcarbonyl, amido and (C1-C6)alkylsulphonyl radicals; and R3 is chosen from C1-C6 alkyl radicals, C1-C6 monohydroxyalkyl radicals, C2-C6 polyhydroxyalkyl radicals, tri(C1-C6)alkylsilane(C1-C6)alkyl radicals, (C1-C6)alkoxy(C1-C6)alkyl radicals and C1-C6 carbamylalkyl radicals.
In one embodiment, R, R7 and R3 are alkyl radicals that may be substituted.
The radical R2 may also be chosen from onium radicals of formula —XP(O)(O—)OCH2CH2N+(CH3)3 wherein X is chosen from oxygen and radicals —NR11, wherein R11 is chosen from hydrogen, C1-C4 alkyl radicals and hydroxyalkyl radicals.
In one embodiment, R2 may also be chosen from guanidine radicals of formula —X—C═NR8—NR9R10, wherein X is chosen from oxygen and a radical —NR11, and R8, R9, R10 and R11, which may be identical or different, are each chosen from hydrogen, C1-C4 alkyl radicals, and hydroxyalkyl radicals. In another embodiment, X is chosen from radicals of —NR11, R8 is a hydrogen and R9 and R10, which may be identical or different, are each chosen from hydrogen and alkyl radicals, for example, a methyl radical.
The pKa of the guanidine radical R2 is such that this substituent is present in cationic form (═NR8H+) under the standard conditions for the oxidation dyeing of hair.
As used herein, the counter-ion may be chosen from halogens such as bromine, chlorine, fluorine and iodine, hydroxides, citrates, succinates, tartrates, lactates, tosylates, mesylates, benzenesulphonates, acetates, a hydrogen sulphate, and C1-C6 alkyl sulphates such as methyl sulphate and ethyl sulphate.
The pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and the addition salts thereof may, for example, be chosen from:
The pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and addition salts thereof may, for example, be chosen from:
According to one embodiment, the linking arm D comprises at least one phosphoryl radical, for example, at least one radical chosen from [1-(4-Amino-phenyl)-pyrrolidin-3-yl]-oxophosphorylcholine and [1-(4-Amino-3-methyl-phenyl)-pyrrolidin-3-yl]-oxophosphorylcholine.
The dye composition disclosed herein comprises, in a medium suitable for dyeing keratin fibers, such as human hair, at least one oxidation base chosen from pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and the addition salts thereof as defined above.
The at least one oxidation base may be present in an amount ranging, for example, from 0.001% to 10% by weight, relative to the total weight of the dye composition, further for example, from 0.005% to 6% by weight, relative to the total weight of the dyeing composition.
The dye composition disclosed herein may further comprise at least one coupler conventionally used for dyeing keratin fibers. The at least one coupler may, for example, be chosen from meta-phenylenediamines, meta-aminophenols, meta-diphenols, naphthalenic couplers and heterocyclic couplers, and the addition salts thereof.
The at least one coupler may, for example, be chosen from 2-methyl-5-aminophenol, 5-N-(β-hydroxyethyl)amino-2-methylphenol, 6-chloro-2-methyl-5-aminophenol, 3-aminophenol, 1,3-dihydroxybenzene, 1,3-dihydroxy-2-methylbenzene, 4-chloro-1,3-dihydroxybenzene, 2,4-diamino-1-(β-hydroxyethyloxy)benzene, 2-amino-4-(β-hydroxyethylamino)-1-methoxybenzene, 1,3-diaminobenzene, 1,3-bis(2,4-diaminophenoxy)propane, 3-ureidoaniline, 3-ureido-1-dimethylaminobenzene, sesamol, 1-β-hydroxyethylamino-3,4-methylenedioxybenzene, α-naphthol, 2-methyl-1-naphthol, 6-hydroxyindole, 4-hydroxyindole, 4-hydroxy-N-methylindole, 2-amino-3-hydroxypyridine, 6-hydroxybenzomorpholine, 3,5-diamino-2,6-dimethoxypyridine, 1-N-(β-hydroxyethyl)amino-3,4-methylenedioxybenze and 2,6-bis(β-hydroxyethylamino)toluene and the acid addition salts thereof.
In one embodiment, the at least one coupler is present in an amount ranging from 0.001% to 10% by weight, relative to the total weight of the dye composition, further for example, from 0.005% to 6% by weight, relative to the total weight of the dye composition.
In another embodiment, the dye composition may also comprise at least one additional oxidation base conventionally used in oxidation dyeing, other than those described above. The at least one additional oxidation base may, for example, be chosen from para-phenylenediamines other than those described above, such as bis(phenyl)alkylenediamines, para-aminophenols, bis-para-aminophenols, ortho-aminophenols and heterocyclic bases, and the addition salts thereof.
The para-phenylenediamines may, for example, be chosen from para-phenylenediamine, para-tolylenediamine, 2-chloro-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, N,N-dimethyl-para-phenylenediamine, N,N-diethyl-para-phenylenediamine, N,N-dipropyl-para-phenylenediamine, 4-amino-N,N-diethyl-3-methylaniline, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 4-N,N-bis(β-hydroxyethyl)amino-2-methylaniline, 4-N,N-bis(β-hydroxyethyl)amino-2-chloroaniline, 2-β-hydroxyethyl-para-phenylenediamine, 2-fluoro-para-phenylenediamine, 2-isopropyl-para-phenylenediamine, N-(β-hydroxypropyl)-para-phenylenediamine, 2-hydroxymethyl-para-phenylenediamine, N,N-dimethyl-3-methyl-para-phenylenediamine, N-ethyl-N-(β-hydroxyethyl)-para-phenylenediamine, N-(β,β-dihydroxypropyl)-para-phenylenediamine, N-(4′-aminophenyl)-para-phenylenediamine, N-phenyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylenediamine, 2-β-acetylaminoethyloxy-para-phenylenediamine, N-(β-methoxyethyl)-para-phenylenediamine, 4-aminophenylpyrrolidine, 2-thienyl-para-phenylenediamine, 2-β-hydroxyethylamino-5-aminotoluene and 3-hydroxy-1-(4′-aminophenyl)pyrrolidine, and the acid addition salts thereof.
The para-phenylenediamines may, for example, be chosen from para-phenylenediamine, para-tolylenediamine, 2-isopropyl-para-phenylenediamine, 2-β-hydroxyethyl-para-phenylenediamine, 2-β-hydroxyethyloxy-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, N,N-bis(β-hydroxyethyl)-para-phenylenediamine, 2-chloro-para-phenylenediamine and 2-β-acetylaminoethyloxy-para-phenylenediamine, and the acid addition salts thereof.
The bis(phenyl)alkylenediamines may be chosen, for example, from N,N′-bis(β-hydroxyethyl)-N,N′-bis(4′-aminophenyl)-1,3-diaminopropanol, N,N′-bis(β-hydroxyethyl)-N,N′-bis(4-aminophenyl)ethlyenediamine, N,N′-bis(4-aminophenyl)tetra-methylenediamine, 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 and 1,8-bis(2,5-diaminophenoxy)-3,6-dioxaoctane, and the acid addition salts thereof.
The para-aminophenols may be chosen, for example, from para-aminophenol, 4-amino-3-methylphenol, 4-amino-3-fluorophenol, 4-amino-3-hydroxymethylphenol, 4-amino-2-methylphenol, 4-amino-2-hydroxymethylphenol, 4-amino-2-methoxymethylphenol, 4-amino-2-aminomethylphenol, 4-amino-2-(β-hydroxyethylaminomethyl)phenol and 4-amino-2-fluorophenol, and the acid addition salts thereof.
The ortho-aminophenols may be chosen, for example, from 2-aminophenol, 2-amino-5-methylphenol, 2-amino-6-methylphenol and 5-acetamido-2-aminophenol, and the acid addition salts thereof.
The heterocyclic bases, may be chosen, for example, from pyridine derivatives, pyrimidine derivatives and pyrazole derivatives.
The pyridine derivatives may be chosen from compounds disclosed, for example, in Patent Nos. GB 1 026 978 and GB 1 153 196, such as 2,5-diaminopyridine, 2-(4-methoxyphenyl)amino-3-aminopyridine, 2,3-diamino-6-methoxypyridine, 2-(β-methoxyethyl)amino-3-amino-6-methoxypyridine and 3,4-diaminopyridine, and the acid addition salts thereof.
The pyridine oxidation bases may also be chosen, for example, from 3-aminopyrazolo[1,5-a]pyridine oxidation bases and the addition salts thereof disclosed, for example, in Patent Application No. FR 2 801 308. For example, the pyridine oxidation bases may be chosen from pyrazolo[1,5-a]pyrid-3-ylamine; 2-acetylaminopyrazolo[1,5-a]pyrid-3-ylamine; 2-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; 3-aminopyrazolo[1,5-a]pyridine-2-carboxylic acid, 2-methoxypyrazolo[1,5-a]pyrid-3-ylamine; (3-aminopyrazolo[1,5-a]pyrid-7-yl)methanol; 2-(3-aminopyrazolo[1,5-a]pyrid-5-yl)ethanol; 2,3-aminopyrazolo[1,5-a]pyrid-7-yl)ethanol; (3-aminopyrazolo[1,5-a]pyrid-2-yl)methanol; 3,6-diaminopyrazolo[1,5-a]pyridine; 3,4-diaminopyrazolo[1,5-a]pyridine; pyrazolo[1,5-a]pyridine-3,7-diamine; 7-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; pyrazolo[1,5-a]pyridine-3,5-diamine; 5-morpholin-4-ylpyrazolo[1,5-a]pyrid-3-ylamine; 2-[(3-aminopyrazolo[1,5-a]pyrid-7-yl)(2-hydroxyethyl)amino]ethanol; 2-[(3-aminopyrazolo[1,5-a]pyrid-7-yl)(2-hydroxyethyl)amino]ethanol; 3-aminopyrazolo-[1,5-a]pyrid-5-ol; 3-aminopyrazolo[1,5-a]pyrid-4-ol; 3-aminopyrazolo[1,5-a]pyrid-6-ol; 3-aminopyrazolo[1,5-a]pyrid-7-ol and the acid and base addition salts thereof.
The pyrimidine derivatives may be chosen, for example, from the compounds disclosed in Patent Nos. DE 2 359 399 and JP 88-169 571; JP 05 63 124; EP 0 770 375 and Patent Application No. WO 96/15765, such as 2,4,5,6-tetraaminopyrimidine, 4-hydroxy-2,5,6-triaminopyrimidine, 2-hydroxy-4,5,6-triaminopyrimidine, 2,4-dihydroxy-5,6-diaminopyrimidine and 2,5,6-triaminopyrimidine, and pyrazolopyrimidine derivatives such as those disclosed in Patent Application FR-A-2 750 048 such as pyrazolo[1,5-a]pyrimidine-3,7-diamine; 2,5-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine; pyrazolo[1,5-a]pyrimidine-3,5-diamine; 2,7-dimethylpyrazolo[1,5-a]pyrimidine-3,5-diamine; 3-aminopyrazolo[1,5-a]pyrimidin-7-ol; 3-aminopyrazolo[1,5-a]pyrimidin-5-ol; 2-(3-aminopyrazolo[1,5-a]pyrimidin-7-ylamino)ethanol, 2-(7-aminopyrazolo[1,5-a]pyrimidin-3-ylamino)ethanol, 2-[(3-aminopyrazolo[1,5-a]pyrimidin-7-yl)(2-hydroxyethyl)amino]ethanol, 2-[(7-aminopyrazolo[1,5-a]pyrimidin-3-yl)(2-hydroxyethyl)amino]ethanol, 5,6-dimethylpyrazolo[1,5-a]pyridine-3,7-diamine, 2,6-dimethylpyrazolo[1,5-a]pyrimidine-3,7-diamine, 2,5,N7,N7-tetramethylpyrazolo[1,5-a]pyrimidine-3,7-diamine and 3-amino-5-methyl-7-imidazolypropylaminopyrazolo[1,5-a]pyrimidine, and the acid addition salts thereof and the tautomeric forms thereof, when a tautomeric equilibrium exists.
The pyrazole derivatives may be chosen from compounds disclosed in Patent Nos. DE 3 843 892 and DE 4 133 957 and Patent Application Nos. WO 94/08969, WO 94/08970, FR-A-2 733 749 and DE 195 43 988, such as 4,5-diamino-1-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)pyrazole, 3,4-diaminopyrazole, 4,5-diamino-1-(4′-chlorobenzyl)pyrazole, 4,5-diamino-1,3-dimethylpyrazole, 4,5-diamino-3-methyl-1-phenylpyrazole, 4,5-diamino-1-methyl-3-phenylpyrazole, 4-amino-1,3-dimethyl-5-hydrazinopyrazole, 1-benzyl-4,5-diamino-3-methylpyrazole, 4,5-diamino-3-tert-butyl-1-methylpyrazole, 4,5-diamino-1-tert-butyl-3-methylpyrazole, 4,5-diamino-1-(β-hydroxyethyl)-3-methylpyrazole, 4,5-diamino-1-ethyl-3-methylpyrazole, 4,5-diamino-1-ethyl-3-(4′-methoxyphenyl)pyrazole, 4,5-diamino-1-ethyl-3-hydroxymethylpyrazole, 4,5-diamino-3-hydroxymethyl-1-methylpyrazole, 4,5-diamino-3-hydroxymethyl-1-isopropylpyrazole, 4,5-diamino-3-methyl-1-isopropylpyrazole, 4-amino-5-(2′-aminoethyl)amino-1,3-dimethylpyrazole, 3,4,5-triaminopyrazole, 1-methyl-3,4,5-triaminopyrazole, 3,5-diamino-1-methyl-4-methylaminopyrazole and 3,5-diamino-4-(β-hydroxyethyl)amino-1-methylpyrazole, and the acid addition salts thereof.
The at least one additional oxidation base may be present in the dye composition in an amount ranging, for example, from 0.001% to 10% by weight, relative to the total weight of the dye composition, further for example, from 0.005% to 6% by weight, relative to the total weight of the composition.
The addition salts of the at least one oxidation base, of the at least one additional oxidation base, and of the at least one coupler may be chosen, for example, from the acid addition salts, such as the hydrochlorides, hydrobromides, sulphates, citrates, succinates, tartrates, lactates, tosylates, benzenesulphonates, phosphates and acetates, and the base addition salts, such as sodium hydroxide, potassium hydroxide, ammonia, amines and alkanolamines.
In another embodiment, the dye composition disclosed herein may also comprise at least one direct dye chosen, for example, from nitrobenzene dyes, azo direct dyes and methine direct dyes. The at least one direct dye may be of nonionic, anionic or cationic nature.
The medium suitable for dyeing, also known as the dye support, comprises water or a mixture of water and at least one organic solvent to dissolve the compounds that are not sufficiently soluble in water. The at least one organic solvent may, for example, be chosen from C1-C4 lower alkanols, such as ethanol and isopropanol; polyols and polyol ethers such as 2-butoxyethanol, propylene glycol, propylene glycol monomethyl ether, diethylene glycol monoethyl ether and monomethyl ether, as well as aromatic alcohols such as benzyl alcohol and phenoxyethanol.
The at least one organic solvent may be present in an amount ranging, for example, from 1% to 40% by weight, relative to the total weight of the dye composition, further for example, from 5% to 30% by weight, relative to the total weight of the dyeing composition.
In another embodiment, the dye composition may also comprise, for example, at least one adjuvant conventionally used in compositions for dyeing the hair. For example, the at least one adjuvant may be chosen from anionic, cationic, nonionic, amphoteric and zwitterionic surfactants, anionic, cationic, nonionic, amphoteric and zwitterionic polymers, inorganic and organic thickeners, for example, anionic, cationic, nonionic and amphoteric associative polymeric thickeners, antioxidants, penetration agents, sequestering agents, fragrances, buffers, dispersing agents, packaging agents, for example, volatile and non-volatile, modified and unmodified silicones, film-forming agents, ceramides, preserving agents and opacifiers.
The at least one adjuvant may be present in an amount ranging, for example, from 0.01% to 20% by weight, relative to the weight of the composition.
A person skilled in the art may choose at least one optional additional compound such that the advantageous properties intrinsically associated with the oxidation dye composition disclosed herein are not, or are not substantially, adversely affected by the addition envisaged.
The pH of the dye composition disclosed herein may range, for example, from 3 to 12, further for example, from 5 to 11. The pH may be adjusted to the desired value using, for example, at least one agent chosen from acidifying and basifying agents. The acidifying agents and the basifying agents may be chosen, for example, from those conventionally used in the dyeing of keratin fibers and standard buffer systems.
The acidifying agents may, for example, be chosen from inorganic and organic acids such as hydrochloric acid, orthophosphoric acid, sulphuric acid, carboxylic acids such as acetic acid, tartaric acid, citric acid and lactic acid, and sulphonic acids.
The basifying agents may, for example, be chosen from aqueous ammonia, alkaline carbonates, alkanolamines such as mono-, di- and triethanolamine and derivatives thereof, sodium hydroxide, potassium hydroxide and the compounds of formula (V) below:
wherein W is chosen from propylene residues optionally substituted with at least one radical chosen from a hydroxyl radical and C1-C4 alkyl radicals; Ra, Rb, Rc and Rd, which may be identical or different, are each chosen from hydrogen, C1-C4 alkyl radicals and C1-C4 hydroxyalkyl radicals.
The dye composition disclosed herein may be in various forms, such as in a form chosen from liquids, creams, gels, and any other form that may be suitable for dyeing keratin fibers, such as human hair.
Further disclosed herein is a process comprising applying the dye composition disclosed herein to keratin fibers, wherein the color may be developed using at least one oxidizing agent. The color may be developed, for example, at acidic, neutral or alkaline pH. The at least one oxidizing agent may be added to the dye composition disclosed herein at the time of use, or an oxidizing composition comprising at least one oxidizing agent may, be applied simultaneously or sequentially to the dye composition disclosed herein.
In one embodiment, the dye composition disclosed herein may be mixed, for example, at the time of use, with an oxidizing composition comprising, in a medium suitable for dyeing, at least one oxidizing agent. The at least one oxidizing agent is present in an amount that is sufficient to develop a coloration. The mixture obtained then may be applied to the keratin fibers. After an action time ranging from 3 to 50 minutes, for example, from 5 to 30 minutes, the keratin fibers may be rinsed, washed with shampoo, rinsed again and then dried.
The at least one oxidizing agent used for the oxidation dyeing of keratin fibers may be chosen, for example, from hydrogen peroxide, urea peroxide, alkali metal bromates, persalts such as perborates and persulphates, peracids and oxidase enzymes, such as peroxidases, 2-electron oxidoreductases such as uricases, and 4-electron oxygenases, such as laccases. In one embodiment, the at least one oxidizing agent is hydrogen peroxide.
The oxidizing composition may also comprise at least one adjuvant chosen from those conventionally used in compositions for dyeing the hair, such as those adjuvants defined above.
The pH of the oxidizing composition comprising the at least one oxidizing agent may be such that, after mixing with the dye composition, the pH of the resulting composition applied to the keratin fibers ranges, for example, from 3 to 12, further for example, from 5 to 11. The pH may be adjusted to the desired value using, for example, at least one agent chosen from acidifying and basifying agents. The acidifying and basifying agents may be chosen from those conventionally used in the dyeing of keratin fibers and standard buffer systems as defined above.
The ready-to-use composition that is finally applied to the keratin fibers may, for example, be in various forms, such as in a form chosen from liquids, creams and gels and any other form that is suitable for dyeing keratin fibers, such as human hair.
Further disclosed herein is a multi-compartment dyeing device or “kit”, comprising a first compartment comprising the dye composition disclosed herein and a second compartment comprising the oxidizing composition. This device may, for example, be equipped with a means for applying the desired mixture to the hair, such as the devices disclosed in Patent No. FR-2 586 913.
Using this device, it is possible to dye keratin fibers using a process comprising mixing a dye composition comprising at least one oxidation base chosen from pyrrolidinyl-substituted para-phenylenediamine derivative of formula (I) and the addition salts thereof with at least one oxidizing agent, and applying the mixture obtained to the keratin fibers for a time that is sufficient to develop the desired coloration.
Even further disclosed herein are nitro pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I′) and the addition salts thereof, such derivatives being intermediate compounds in the synthesis of pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I).
wherein R1, n and R2 are previously defined herein.
The pyrrolidinyl-substituted para-phenylenediamine derivatives of formula (I) and the addition salts thereof as disclosed herein can be prepared by the application or adaptation of known methods. For example, they can be obtained by the adaptation of the methods disclosed below.
The examples that follow serve to illustrate the invention without, however, being limiting in nature.
Synthesis of 1-(4-nitrophenyl)pyrrolidin-3-ol (1)
2 g of 1-fluoro-4-nitrobenzene (0.0155 mol), 1.3 g of sodium hydrogen carbonate (0.0155 mol) and 15 ml of a dioxane/water mixture (8/2) were placed in a three-necked flask. 1.35 g of 3-pyrrolidinol (0.0155 mol) was rapidly added to this mixture. The heterogeneous mixture was heated at reflux (87° C.) for 10 hours. The reaction mixture was then poured into ice-water; a yellow precipitate was obtained, which was filtered off and rinsed with water. After drying under vacuum in the presence of P2O5, 2.95 g of a yellow solid are obtained (97% yield).
1H NMR (DMSO-d6, 200 MHz, ppm) in accordance with the expected product: 8.04 (d, J=9 Hz, 2H); 6.58 (d, J=9 Hz, 2H); 5.06 (d, J=3.6 Hz, 1H); 4.41 (m, 1H); 3.45 (m, 3H); 3.20 (m, 1H); 2.04 (m, 2H).
Synthesis of 1-(4-aminophenyl)pyrrolidin-3-yl methanesulphonate (2)
40 ml (0.516 mol) of mesyl chloride was added dropwise at 5° C. to 83.3 g (0.4 mol) of N-(4-nitrophenly)-3-hydroxypyrrolidine (1) dissolved in 625 ml of anhydrous THF and 72.7 ml (0.6 mol) of triethylamine. The mixture was allowed to return to room temperature and was then poured onto ice. After filtering off the precipitate by suction and drying, 109 g of yellow powder (2) was obtained.
Melting point: 203° C.
1H NMR (400 MHz-DMSO) ppm 8.09 (d, 2H); 6.68 (d, 2H); 5.47 (m,1H); 3.77-3.48 (m, 4H); 3.28 (s, 3H); 2.35 (m, 2H).
ESI+MASS: m/z=287 [MH+].
Synthesis of 1 -methyl-3-[1-(4-nitrophenyl)pyrrolidin-3-yl]-3H-imidazol-1-ium methanesulphonate (3)
23 g (0.08 mol) of 1-(4-nitrophenyl)pyrrolidin-3-yl methanesulphonate (2) was heated for 8 hours at 85° C. in 150 g of 1-methylimidazole (1.82 mol). This solution was stirred in 2 l of ethyl acetate to the point of crystallization. After filtration and drying, 24 g of yellow powder (3) was obtained.
1H NMR (400 MHz-DMSO) ppm 9.44 (s, 1H); 8.29 (d, 2H); 8.07 (m, 1H); 7.96 (m, 1H); 6.91 (d, 2H); 5.48 (m, 1H); 4.16 (m, 1H); 4.02 (s, 3H) from 3.98 to 3.79 (m, 4H); 2.85 (m, 1H); 2.69 (m, 1H); 2.50 (s, 3H).
ESI+mass: m/z=273 [M+].
Synthesis of 1-methyl-3-[1-(4-nitrophenyl)pyrrolidin-3-yl]-3H-imidazol-1-ium chloride (4)
23 g (0.0624 mol) of 1-methyl-3-[1-(4-nitrophenyl)pyrrolidin-3-yl]-3H-imidazol-1-ium methanesulphonate (3) dissolved in 200 ml of water was stirred with 500 g of Amberlite IRA-402 ion-exchange resins for 14 hours; the resin was separated out by filtration and the filtrate was concentrated and then taken up in isopropanol. The yellow powder was recovered by filtration and then dried. 16.5 g of 1-methyl-3-[1-(4-nitrophenyl)pyrrolidin-3-yl]-3H-imidazol-1-ium chloride (4) was obtained.
1H NMR (400 MHz-DMSO) ppm 9.35 (s, 1H); 8.11 (m, 2H); 8.90 (m, 1H); 7.78 (m, 1H); 6.71 (m, 2H); 5.31 (m, 1H); 4.37 (m, 1H); from 3.98 to 3.95 (m, 1H); 3.85 (s, 3H); from 3.83 to 3.69 (m, 4H); from 2.51 to 2.49 (m, 2H);
ESI+mass: m/z=307 [M+].
Synthesis of 1-methyl-3-[1-(4-aminophenyl)pyrrolidin-3-yl]-1H-imidazol-1-ium chloride hydrochloride (5)
16 g (0.0518 mol) of the preceding derivative (4) dissolved in 600 ml of ethanol was hydrogenated in the presence of palladium-on-charcoal under a hydrogen pressure of 8 bar. After filtering off the catalyst, the expected derivative (5) was isolated in the form of the hydrochloride.
1H NMR (400 MHz-DMSO) ppm 8.86 (s, 1H); 7.59 (t, 1H); 7.54 (t, 1H); 7.41 (m, 2H); 6.89 (m, 2H); 5.33 (m, 1H); 3.97 (m, 3H); 3.85 (m, 2H); 3.71 (m, 1H); 3.50 (m, 1H); 2.76 (m, 1H); 2.51 (m, 1H);
ESI+mass: m/z=243 [M+].
Synthesis of 1′-(4-Nitro-phenyl)-[1,3′]bipyrrolidinyl (1)
5 g (0.0174 mole) of methanesulfonic acid 1-(4-nitro-phenyl)-pyrrolidin-3yl ester (2) were heated 2 hours at 85° C. in 30 ml of pyrrolidine. The mixture was then poured on ice water until crystallization occurred. After filtrating and drying, the obtained yellow powder was chromatographed with an eluent consisting of dichloromethane/methanol (98/2). 2.6 g of derivative (1) was thus obtained (yield 53%).
melting point=114° C.
RMN 1H (400 MHz, DMSO) ppm 8.04 (m, 2H); 6.61 (m, 2H); 3.60(m, 2H); 3.40(m, 1H); 3.24 (m, 1H); 2.86 (m,1H); 2.50 (m, 2H); 2.16 (m, 1H); 1.92 (m, 1H); 1.70 (m, 4H).
ESI+Mass: m/z=262(MH+)
Synthesis of 1-Methyl-1′-(4-nitro-phenyl)-[1,3′]bipyrrolidinyl-1-ium; chloride (3)
24.8 g (0.095 mole) of 1′-(4-Nitro-phenyl)-[1,3′]bipyrrolidinyl (1) were mixed with 330 ml of ethylacetate. 10 ml (0.105 mole) of dimethylsulfate were added and the mixture was heated at reflux for 4 hours. At ambient temperature, the yellow powder thus obtained was filtered off, washed with ethyl acetate and dried under vacuum. The ions were exchanged on Amberlite IRA-402 resin. 21 g of a yellow powder were obtained (3) (yield 75%).
RMN 1H (400 MHz, D2O) ppm 7.96 (m, 2H); 6.51 (m, 2H); 4.3 (m, 1H); 3.78-3.39 (m, 8H); 2.98 (s,3H); 2.97-2.42 (m, 2H); 2.16 (m, 4H).
ESI+Mass: m/z=276(M+)
Synthesis of 1′-(4-Amino-phenyl)-1-methyl-[1,3′]bipyrrolidinyl-1-ium chloride, hydrochloride (4)
21 g (0.067 mole) of the preceding derivative (3) in 700 ml of ethanol was hydrogenated in presence of palladium on charcoal under hydrogen pressure of 10 bars; after filtration of the catalyst, the derivative (4) was isolated under hydrochloride form.
RMN 1H (400 MHz, DMSO) ppm 2,29 (m, 4H); 2,49 (m, 1H); 2,63 (m, 1H); 3,1 (s, 3H); 3,35 (m, 1H); 3,69 (m, 7H); 3,8 (dd, 1H); 4,42 (m, 1H); 6,86 (m, 2H); 7,35 (m, 2H).
ESI+Mass: m/z=246(M+)
Synthesis of 1-(3-Methyl-4-nitro-phenyl)-pyrrolidin-3-ol (1)
In a three necked flask, 38.78 g of 5-fluoro-2-nitrotoluene (0.25 mol), 41.4 g of potassium carbonate (0.3 mol) and 200 ml of N-methylpyrrolidinone were mixed. 26.13 g of 3-pyrrolidinol (0.3 mol) were added to this mixture. The heterogeneous mixture was agitated at ambient temperature for 12 hours. The reacting mixture was then poured on ice water. A yellow powder was then obtained. The powder was then filtered off and rinsed with water. After drying under vacuum with P2O5, 55.56 g of a yellow solid were obtained (yield) (95%).
RMN 1H (400 MHz-DMSO) ppm 8.01 (d, 1H); 6.50-6.46 (m, 2H); 5.04 (m, 1H); 4.42 (m, 1H) 3.50-3.42 (m, 3H); 3.24-3.21 (m, 1H); 2.56 (s, 3H); 2.15-1.90 (m, 2H).
Synthesis of 1-(3-methyl-4-nitro-phenyl)-pyrrolidin-3-yl methane sulfonic ester (2)
35.56 g (0.16 mole) of 1-(3-Methyl-4-nitro-phenyl)-pyrrolidin-3-ol (1) in 500 ml of anhydrous THF and 29 ml (0.24 mole) of triethylamine were mixed drop to drop with 16 ml (0.21 mole) of mesyl chloride at 5° C.
At ambient temperature, the mixture was agitated for 1 hour then poured on ice water. After filtering and drying, 48 g of a yellow powder were obtained (2).
RMN 1H (400 MHz-DMSO) ppm 7.98-7.95 (m, 1H); 6.50-6.47 (m, 2H); 5.4 (m, 1H); 3.64-3.39 (m, 4H); 3.21 (s, 3H); 2.50 (s, 3H); 2.27-2.24 (m, 2H).
Synthesis of 1-Methyl-3-[1-(3-methyl-4-nitro-phenyl)-pyrrolidin-3-yl]-3H-imidazol-1-ium methanesulfonate (3)
6 g (0.02 mole) of 1-(3-methyl-4-nitro-phenyl)-pyrrolidin-3-yl methane sulfonic ester (2) were heated 12 hours at 90° C. in 30 ml of 1-methylimidazole. The solution was agitated in 2 l of ethylacetate until crystallization. After filtering off and drying, 6.6 g of a yellow powder were obtained (3).
RMN 1H (400 MHz-DMSO) ppm 8.07 (s, 1H); 7.72 (m, 1H); 7.43 (s, 1H); 7.42 (m, 1H); 6.28-6.23 (m, 2H); 5.16 (m, 1H); 3.81-3.77 (m, 4H); 3.67-3.43 (m, 3H); 2.68 (s, 3H); 2.59 (m 1H); 2.35 (m, 1H); 2.28 (s, 3H).
ESI+Mass: m/z=287[M+]
Synthesis of 1-Methyl-3-[1-(3-methyl-4-nitro-phenyl)-pyrrolidin-3-yl]-3H-imidazol-1-ium chloride (4)
6.5 g (0.017 mole) of 1-Methyl-3-[1-(3-methyl-4-nitro-phenyl)-pyrrolidin-3-yl]-3H-imidazol-1-ium methanesulfonate (3) in 200 ml of water were agitated with 200 g of an ion-exchange resin Amberlite IRA-402 for 12 hours. The resin was separated by filtration, the filtrate was concentrated then mixed with isopropanol. A yellow powder was then obtained after filtering off and drying (3.4 g).
RMN 1H (400 MHz-DMSO) ppm 8.72 (s, 1H); 7.65 (m, 1H); 7.43 (s, 1H); 7.37 (m, 1H); 6.22-6.17 (m, 2H); 5.16 (m, 1H); 3.78 (m, 4H); 3.64-3.40 (m, 3H); 2.60-2.56 (m, 1H); 2.40-2.37 (m, 1H); 2.23 (s, 3H).
ESI+Mass: m/z=287[M+]
Synthesis of 1-methyl-3-[1-(3-methyl-4-amino-phenyl)-pyrrolidin-3-yl]-3H-imidazol-1-ium chloride, hydrochloride (5)
3.2 g (0.01 mole) of derivative (4) in 300 ml of ethanol were hydrogenated in the presence of palladium on charcoal under hydrogen pressure of 9 bars. The catalyst was removed by filtration. The derivative (5) was isolated under chloride form.
RMN 1H (400 MHz-DMSO) ppm 7,35 (m, 2H); 6,86 (m, 2H); 4,42 (m, 1H); 3,8 (dd, 1H); 3,69 (m, 7H); 3,35 (m, 1H); 3,1 (s, 3H); 2,63 (m,1H); 2,49 (m, 1H); 2,29 (m, 4H).
ESI+Mass: m/z=257[M+]
Synthesis of N-[1-(4-nitrophenyl)pyrrolidin-3-yl]acetamide (1)
After dissolving 56.4 g of 1-fluoro-4-nitrobenzene (0.4 mol) and 51.2 g of 3-acetamidopyrrolidine (0.4 mol) in 400 ml of NMP, 66.4 g of potassium carbonate (0.48 mol) were added under a nitrogen atmosphere and the mixture was heated at 100° C. for 18 hours. The reaction medium was allowed to cool and was then poured into 2 l of water. The yellow precipitate formed was filtered off, washed with water and then dried in a vacuum oven over P2O5. 100 g (100%) of N-[1-(4-nitrophenyl)pyrrolidin-3-yl]acetamide (1) was thus obtained in the form of a yellow solid.
Synthesis of 1-(4-nitrophenyl)pyrrolidin-4-ylamine (2)
100 g (0.4 mol) of N-[1-(4-nitrophenyl)pyrrolidin-3-yl]acetamide (1) was placed in suspension in a solution containing 300 ml of 37% hydrochloric acid and 660 ml of water in a 2 l three-necked flask. The reaction medium was heated at 90° C. for 7 hours 45 minutes. After cooling, the medium was neutralized gently with 300 ml of aqueous 35% sodium hydroxide (pH=8 approximately). The resulting solid was subsequently filtered off and then washed with water until the washing waters were neutral. The product was then dried under vacuum over P2O5. 74 g (89%) of 1-(4-nitrophenyl)pyrrolidin-4-ylamine (2) was thus obtained in the form of a yellow solid.
Synthesis of N-[1-(4-nitrophenyl)pyrrolidin-3-yl]guanidine (3)
2.07 g (0.01 mol) of [1-(4-nitrophenyl)pyrrolidin-3-yl]amine (2) was heated to 90° C. in 10 ml of DMF. 1.32 g (0.0009 mol) of 1-amidinopyrazole monohydrochloride was added slowly to the reaction medium. The mixture was heated for 8 hours. A yellow solid was thus precipitated. The solid thus obtained was filtered off, washed with ethanol and dried under vacuum to give 2 g of a yellow powder (3) (70%).
1H NMR (400 MHz, DMSO) ppm 8.08 (m, 2H), 6.66 (m, 2H), 4.34 (m, 1H), 3.72 (m, 2H), 3.56 (m, 1H), 3.48 (m, 1H), 3.33 (m, 1H), 2.31 (m, 1H), 2.02 (m, 1H).
ESI+mass: m/z=250 (MH+).
Synthesis of N-[1-(4-aminophenyl)pyrrolidin-3-yl]guanidine trihydrochloride (4)
1.8 g (0.063 mol) of the preceding derivative (3) dissolved in 50 ml of ethanol and 550 ml of water were hydrogenated in the presence of palladium-on-charcoal under a hydrogen pressure of 8 bar; after filtering off the catalyst, the expected derivative (4) was isolated in the form of the hydrochloride (60%).
1H NMR (400 MHz, DMSO) ppm 7.52 (m, 2H), 7.31 (m, 2H), 4.53 (m,1H), 3.94 (dd, 1H), 3.84 (m, 1H), 3.72 (m, 2H), 2.64 (m, 1H), 2.28 (m, 1H).
ESI+mass: m/z=220 (MH+).
Synthesis of 3-[1-(4-nitrophenyl)pyrrolidin-3-yl]-1,3-thiazol-3-ium methanesulfonate (1)
1.14 g of 1-(4-nitrophenyl)pyrrolidin-3-yl methanesulfonate (0.004 mol), 0.01 g of sodium iodate and 5 g (0.059 mol) of thiazole were placed in a three-necked flask. The heterogeneous mixtures was heated at 110° C. for 18 hours. The reaction mixture was then poured into 100 ml of ethylacetate; a yellow precipitate was then obtained which was filtered off and rinsed with water. After drying under vacuum in the presence of P2O5, 1 g of a yellow solid was obtained. The obtained yellow solid was then recrystallized in isopropanol.
RMN 1H (400 MHz-DMSO) ppm) 10,26 (dd, 1H); 8,64 (dd, 1H); 8,41 (dd 1H); 8,12 (m ,2H); 6,74 (m, 2H); 5,72 (m, 1H); 4,05 (dd, 1H); 3,95 (dd, 1H); 3,76 (m, 1H ); 3,62 (m, 1H); 2,76 (m, 1H); 2,6 (m, 1H); 2,31 (s, 3H).
ESI+Mass: m/z=270[M+].
Synthesis of 3-[1-(4-Amino-phenyl)-pyrrolidin-3-yl]-thiazol-3-ium acetate (2)
After reducing with zinc/acetic acid, 1-[1-(4-aminophenyl)pyrrolidin-3-yl]thyazolium chloride was obtained.
ESI+Mass: m/z=246[M+].
Synthesis of 1-[1-(4-Nitro-phenyl)-pyrrolidin-3-yl]-pyridinium chloride (1)
7 g of 1-(4-nitrophenyl)pyrrolidin-3-yl methanesulfonate (0.0244 mol) and 60 ml of pyridin were placed in a three-necked flask. The mixture was heated at 100° C. for 16 hours. The precipitate was filtered off. After washing with ether and drying, 8.5 g of a yellow powder was obtained. The powder was solubilized in 200 ml of water, the solution was then passed through a IRA402 resin. After evaporating and drying, 5.4 g of 1-[1-(4-nitrophenyl)pyrrolidin-3-yl]pyridinium chloride was obtained. (1)
RMN 1H (400 MHz-DMSO) ppm 9,26 (m, 2H); 8,67 (m, 1H); 8,2 (m, 2H); 8,1 (m, 2H); 6,74 (m, 1H); 5,86 (m, 1H); 4,03 (dd, 1H); 3,84 (m, 1H); 3,62 (m, 1H); 2,84 (m, 1H); 2,67 (m, 1H).
ESI+Mass: m/z=270[M+].
Synthesis of 1-[1-(4-Amino-phenyl)-pyrrolidin-3-yl]-pyridinium acetate (2)
After reducing with zinc/acetic acid, 1-[1-(4-Amino-phenyl)-pyrrolidin-3-yl]-pyridinium acetate was obtained.(2)
ESI+Mass: m/z=240[M+].
Synthesis of 1-[1-(4-nitrophenyl)pyrrolidin-3-yl]-4-aza-1-azoniabicyclo[2,2,2]octane; methanesulfonate
4.3 g of 1-(4-nitrophenyl)pyrrolidin-3-yl methanesulfonate (0.015 mol), 15 ml of methylethylacetone and 0.56 g (0.005 mol) of 1,4 diazabicyclo-2,2,2-octane were placed in a three-necked flask. The heterogeneous mixture was heated at 95° C. for 10 hours. The reaction mixture was then poured into 150 ml of water; the mixture was filtered off, the aqueous phase was extracted with butanol then concentrated; 0.8 g of a yellow powder was thus obtained after drying corresponding to 1-[1-(4-nitrophenyl)pyrrolidin-3-yl]-4-aza-1-azoniabicyclo[2,2,2]octane; methanesulfonate (1).
RMN 1H (400 MHz-DMSO) ppm 8,14 (d, 2H); 6,72 (d, 2H); 3,67-4,26 (m, 4H); 3,41 (m, 7H); 3,06 (m, 6H); 2,35-2,56 (m, 4H); 2,30 (s, 3H).
ESI+Mass: m/z=303[M+].
Synthesis of 1-[1-(4-Amino-phenyl)-pyrrolidin-3-yl]-4-aza-1-azonia-bicyclo[2,2,2]octane; methanesulfonate; hydrochloride
0.180 g of 1-[1-(4-nitrophenyl)pyrrolidin-3-yl]-4-aza-1-azoniabicyclo[2,2,2]octane; methanesulfonate was hydrogenated under hydrogen pressure of 10 bars in the presence of palladium-on-charcoal in ethanol. After filtrating off the catalyst, the expected derivative (2) was isolated under the hydrochloride form.
RMN 1H (400 MHz-D2O) ppm 7,35 (m, 2H); 6,88 (m, 2H); 4,6 (m, 1H); 4,11 (t, 6H); 4,02 (m, 2H); 3,96 (t, 6H); 3,74 (m, 2H); 2,8 (s, 3H); 2,66 (m, 2H).
ESI+Mass: m/z=373[M+].
The synthesis of 1-(4-amino-phenyl)-pyrrolidin-3-yl]-oxophosphorylcholine derivatives was carried out from 1-(4-Nitro-phenyl)-pyrrolidin-3-ol compound under the protocol disclosed in S. F. Martin, J. Org. Chem. 1994, 59, 4805-4820.
The following compositions 1 to 20 were prepared. The amounts of each base and coupler are listed in moles (1×10−3 moles) relative to the total composition.
At the time of use, the composition was mixed with an equal weight of 20-volumes aqueous hydrogen peroxide solution (6% by weight). The final pH was 9.5.
Each mixture was applied on locks of grey hair comprising 90% of white hairs. After an action of time of 30 minutes, the locks were rinsed, washed with a standard shampoo, rinsed again and dried.
The following results were obtained.
The following compositions 21 to 46 were prepared:
At the time of use, the composition was mixed with an equal weight of 20-volumes aqueous hydrogen peroxide solution (6% by weight). The final pH was 9.5.
Each mixture was applied on locks of grey hair comprising 90% white hairs. After an action of time of 30 minutes, the locks were rinsed, washed with a standard shampoo, rinsed again and dried.
The following results were obtained.
| Number | Date | Country | Kind |
|---|---|---|---|
| 02 03847 | Mar 2002 | FR | national |
This application claims benefit of U.S. Provisional Application No. 60/387,499, filed Jun. 11, 2002.
| Number | Name | Date | Kind |
|---|---|---|---|
| 2261002 | Ritter | Oct 1941 | A |
| 2271378 | Searle | Jan 1942 | A |
| 2273780 | Dittmar | Feb 1942 | A |
| 2375853 | Kirby et al. | May 1945 | A |
| 2388614 | Kirby et al. | Nov 1945 | A |
| 2454547 | Bock et al. | Nov 1948 | A |
| 3061432 | Menzel et al. | Oct 1962 | A |
| 3206462 | McCarty | Sep 1965 | A |
| 3227554 | Barr et al. | Jan 1966 | A |
| 3419391 | Young | Dec 1968 | A |
| 3725067 | Bailey et al. | Apr 1973 | A |
| 3758309 | Bailey et al. | Sep 1973 | A |
| 3874870 | Green et al. | Apr 1975 | A |
| 3915921 | Schlatzer, Jr. | Oct 1975 | A |
| 3926631 | Arai et al. | Dec 1975 | A |
| 3929990 | Green et al. | Dec 1975 | A |
| 3966904 | Green et al. | Jun 1976 | A |
| 4001432 | Green et al. | Jan 1977 | A |
| 4003699 | Rose et al. | Jan 1977 | A |
| 4005193 | Green et al. | Jan 1977 | A |
| 4025617 | Green et al. | May 1977 | A |
| 4025627 | Green et al. | May 1977 | A |
| 4025653 | Green et al. | May 1977 | A |
| 4026945 | Green et al. | May 1977 | A |
| 4027020 | Green et al. | May 1977 | A |
| 4128425 | Greenwald | Dec 1978 | A |
| 4157388 | Christiansen | Jun 1979 | A |
| 4349532 | Vanlerberghe et al. | Sep 1982 | A |
| 4390689 | Jacquet et al. | Jun 1983 | A |
| 4500548 | Silva | Feb 1985 | A |
| 4500630 | Sato et al. | Feb 1985 | A |
| 4509949 | Huang et al. | Apr 1985 | A |
| 4540654 | Sato et al. | Sep 1985 | A |
| 4608250 | Jacquet et al. | Aug 1986 | A |
| 4621046 | Sato et al. | Nov 1986 | A |
| 4702906 | Jacquet et al. | Oct 1987 | A |
| 4719282 | Nadolsky et al. | Jan 1988 | A |
| 4823985 | Grollier et al. | Apr 1989 | A |
| 4842849 | Grollier et al. | Jun 1989 | A |
| 5061289 | Clausen et al. | Oct 1991 | A |
| 5135543 | Chan et al. | Aug 1992 | A |
| 5196189 | Jacquet et al. | Mar 1993 | A |
| 5256526 | Suzuki et al. | Oct 1993 | A |
| 5278034 | Ohki et al. | Jan 1994 | A |
| 5380340 | Neunhoeffer et al. | Jan 1995 | A |
| 5441863 | Tang et al. | Aug 1995 | A |
| 5457210 | Kim et al. | Oct 1995 | A |
| 5538516 | Audousset et al. | Jul 1996 | A |
| 5707786 | Schmuck et al. | Jan 1998 | A |
| 5708151 | Mockli | Jan 1998 | A |
| 5735908 | Cotteret et al. | Apr 1998 | A |
| 5766576 | Löwe et al. | Jun 1998 | A |
| 5769903 | Audousset et al. | Jun 1998 | A |
| 5785717 | Maubru et al. | Jul 1998 | A |
| 5851237 | Anderson et al. | Dec 1998 | A |
| 5876464 | Lim et al. | Mar 1999 | A |
| 5993491 | Lim et al. | Nov 1999 | A |
| 6042620 | Braun et al. | Mar 2000 | A |
| 6099592 | Vidal et al. | Aug 2000 | A |
| 6099593 | Terranova et al. | Aug 2000 | A |
| 6165230 | Rose et al. | Dec 2000 | A |
| 6461391 | Lim et al. | Oct 2002 | B1 |
| 8464731 | Genet et al. | Oct 2002 | |
| 6521761 | Lim et al. | Feb 2003 | B2 |
| 6613313 | Kimura | Sep 2003 | B2 |
| 6638321 | Genet et al. | Oct 2003 | B1 |
| 20020197223 | Kimura | Dec 2002 | A1 |
| 20030093866 | Vidal et al. | May 2003 | A1 |
| 20030150066 | Richard | Aug 2003 | A1 |
| 20040064902 | Sabelle et al. | Apr 2004 | A1 |
| 20040074013 | Terranova et al. | Apr 2004 | A1 |
| 20040078905 | Terranova et al. | Apr 2004 | A1 |
| 20040083559 | Sabelle et al. | May 2004 | A1 |
| 20040088799 | Sabelle et al. | May 2004 | A1 |
| Number | Date | Country |
|---|---|---|
| 23 59 399 | Jan 1975 | DE |
| 38 43 892 | Jun 1990 | DE |
| 41 33 957 | Apr 1993 | DE |
| 42 34 886 | Apr 1994 | DE |
| 42 41 532 | Jun 1994 | DE |
| 299 01 593 | Apr 1999 | DE |
| 195 43 988 | May 1999 | DE |
| 299 02 262 | May 1999 | DE |
| 100 34 617 | Jan 2002 | DE |
| 0 119 860 | Sep 1984 | EP |
| 0 122 324 | Oct 1984 | EP |
| 0 173 109 | Mar 1986 | EP |
| 0 216 479 | Apr 1987 | EP |
| 0 244 160 | Nov 1987 | EP |
| 0 285 274 | Oct 1988 | EP |
| 0 304 001 | Feb 1989 | EP |
| 0 456 226 | Nov 1991 | EP |
| 0 488 248 | Jun 1992 | EP |
| 0 488 909 | Jun 1992 | EP |
| 0 518 238 | Dec 1992 | EP |
| 0 557 851 | Sep 1993 | EP |
| 0 578 248 | Jan 1994 | EP |
| 0 714 954 | Jun 1996 | EP |
| 0 770 375 | May 1997 | EP |
| 0 943 614 | Sep 1999 | EP |
| 0 962 452 | Dec 1999 | EP |
| 1 018 508 | Jul 2000 | EP |
| 1 400 366 | Apr 1965 | FR |
| 2 075 583 | Oct 1971 | FR |
| 2 270 846 | Dec 1975 | FR |
| 2 316 271 | Jan 1977 | FR |
| 2 320 330 | Mar 1977 | FR |
| 2 336 434 | Jul 1977 | FR |
| 2 413 907 | Aug 1979 | FR |
| 2 586 913 | Mar 1987 | FR |
| 2 733 749 | Nov 1996 | FR |
| 2 750 048 | Dec 1997 | FR |
| 2 766 178 | Jan 1999 | FR |
| 2 801 308 | May 2001 | FR |
| 1 021 400 | Mar 1966 | GB |
| 1 026 978 | Apr 1966 | GB |
| 1 153 196 | May 1969 | GB |
| 1 458 377 | Dec 1976 | GB |
| 169571 | Jul 1988 | GB |
| 2 239 265 | Jun 1991 | GB |
| 58-42045 | Mar 1983 | JP |
| 59-98437 | Jun 1984 | JP |
| 59-99437 | Jun 1984 | JP |
| 59-162548 | Sep 1984 | JP |
| 59-171956 | Sep 1984 | JP |
| 60-33552 | Feb 1985 | JP |
| 60-43659 | Mar 1985 | JP |
| 60-172982 | Sep 1985 | JP |
| 60-190779 | Sep 1985 | JP |
| 62-279337 | Dec 1987 | JP |
| 1-115048 | May 1989 | JP |
| 2-19576 | Jan 1990 | JP |
| 5-163124 | Jun 1993 | JP |
| 6-236011 | Aug 1994 | JP |
| 7-36159 | Feb 1995 | JP |
| 7-84348 | Mar 1995 | JP |
| 7-92632 | Apr 1995 | JP |
| 7-98489 | Apr 1995 | JP |
| 7-244361 | Sep 1995 | JP |
| 7-325375 | Dec 1995 | JP |
| 11-158048 | Jun 1999 | JP |
| WO 9408969 | Apr 1994 | WO |
| WO 9408970 | Apr 1994 | WO |
| WO 9501772 | Jan 1995 | WO |
| WO 9515144 | Jun 1995 | WO |
| WO 9615765 | May 1996 | WO |
| WO 9801106 | Jan 1998 | WO |
| WO 9838175 | Sep 1998 | WO |
| WO 9903819 | Jan 1999 | WO |
| WO09917725 | Apr 1999 | WO |
| WO 9964417 | Dec 1999 | WO |
| WO 0168043 | Sep 2001 | WO |
| WO 0245675 | Jun 2002 | WO |
| Number | Date | Country | |
|---|---|---|---|
| 20030229949 A1 | Dec 2003 | US | |
| 20040194227 A9 | Dec 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| 60387499 | Jun 2002 | US |
