CN1486170A - 用于氧化性染发的新的偶合剂 - Google Patents
用于氧化性染发的新的偶合剂 Download PDFInfo
- Publication number
- CN1486170A CN1486170A CNA028037227A CN02803722A CN1486170A CN 1486170 A CN1486170 A CN 1486170A CN A028037227 A CNA028037227 A CN A028037227A CN 02803722 A CN02803722 A CN 02803722A CN 1486170 A CN1486170 A CN 1486170A
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- CN
- China
- Prior art keywords
- amino
- methyl
- phenol
- hair
- ethanol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
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- 210000004209 hair Anatomy 0.000 title claims abstract description 57
- 238000004043 dyeing Methods 0.000 title claims abstract description 21
- 230000001590 oxidative effect Effects 0.000 title abstract description 11
- 239000000203 mixture Substances 0.000 claims abstract description 121
- 230000037308 hair color Effects 0.000 claims abstract description 82
- 150000001875 compounds Chemical class 0.000 claims abstract description 49
- -1 2, 4-diaminophenoxy moieties Chemical group 0.000 claims abstract description 29
- 125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 8
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 17
- 239000007800 oxidant agent Substances 0.000 claims description 16
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 15
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 14
- 239000000118 hair dye Substances 0.000 claims description 13
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 229960001755 resorcinol Drugs 0.000 claims description 11
- 239000004615 ingredient Substances 0.000 claims description 10
- 229940018563 3-aminophenol Drugs 0.000 claims description 9
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 claims description 9
- 238000002156 mixing Methods 0.000 claims description 9
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 8
- XAWPKHNOFIWWNZ-UHFFFAOYSA-N 1h-indol-6-ol Chemical compound OC1=CC=C2C=CNC2=C1 XAWPKHNOFIWWNZ-UHFFFAOYSA-N 0.000 claims description 8
- WCPGNFONICRLCL-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol Chemical compound NC1=CC=C(OCCO)C(N)=C1 WCPGNFONICRLCL-UHFFFAOYSA-N 0.000 claims description 8
- SBUMIGFDXJIPLE-UHFFFAOYSA-N 2-(3-amino-4-methoxyanilino)ethanol Chemical compound COC1=CC=C(NCCO)C=C1N SBUMIGFDXJIPLE-UHFFFAOYSA-N 0.000 claims description 8
- PBBRFJWECSDSDZ-UHFFFAOYSA-N 2-[2,4-diamino-5-(2-hydroxyethoxy)phenoxy]ethanol Chemical compound NC1=CC(N)=C(OCCO)C=C1OCCO PBBRFJWECSDSDZ-UHFFFAOYSA-N 0.000 claims description 8
- BMTSZVZQNMNPCT-UHFFFAOYSA-N 2-aminopyridin-3-ol Chemical compound NC1=NC=CC=C1O BMTSZVZQNMNPCT-UHFFFAOYSA-N 0.000 claims description 8
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 claims description 8
- URWKQPHSJZKEOB-UHFFFAOYSA-N 3-(2,4-diaminophenoxy)propan-1-ol Chemical compound NC1=CC=C(OCCCO)C(N)=C1 URWKQPHSJZKEOB-UHFFFAOYSA-N 0.000 claims description 8
- FLROJJGKUKLCAE-UHFFFAOYSA-N 3-amino-2-methylphenol Chemical compound CC1=C(N)C=CC=C1O FLROJJGKUKLCAE-UHFFFAOYSA-N 0.000 claims description 8
- YGRFRBUGAPOJDU-UHFFFAOYSA-N 5-(2-hydroxyethylamino)-2-methylphenol Chemical compound CC1=CC=C(NCCO)C=C1O YGRFRBUGAPOJDU-UHFFFAOYSA-N 0.000 claims description 8
- ZTMADXFOCUXMJE-UHFFFAOYSA-N 2-methylbenzene-1,3-diol Chemical compound CC1=C(O)C=CC=C1O ZTMADXFOCUXMJE-UHFFFAOYSA-N 0.000 claims description 7
- 239000007822 coupling agent Substances 0.000 claims description 7
- YCIMNLLNPGFGHC-UHFFFAOYSA-N o-dihydroxy-benzene Natural products OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 claims description 7
- ISCYHXYLVTWDJT-UHFFFAOYSA-N 2-[4-amino-n-(2-hydroxyethyl)anilino]ethanol Chemical compound NC1=CC=C(N(CCO)CCO)C=C1 ISCYHXYLVTWDJT-UHFFFAOYSA-N 0.000 claims description 6
- OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 6
- SRJCJJKWVSSELL-UHFFFAOYSA-N 2-methylnaphthalen-1-ol Chemical compound C1=CC=CC2=C(O)C(C)=CC=C21 SRJCJJKWVSSELL-UHFFFAOYSA-N 0.000 claims description 6
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 claims description 6
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims description 6
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 claims description 5
- QQCNRMGYJWTLHB-UHFFFAOYSA-N 4-methyl-2-phenyl-4h-pyrazol-3-one Chemical compound O=C1C(C)C=NN1C1=CC=CC=C1 QQCNRMGYJWTLHB-UHFFFAOYSA-N 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- BKEFUBHXUTWQED-UHFFFAOYSA-N n-(4-amino-3-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(N)C(O)=C1 BKEFUBHXUTWQED-UHFFFAOYSA-N 0.000 claims description 5
- HHVMYUPMJJDVPG-UHFFFAOYSA-N 1-(2,5-diaminophenyl)ethanol Chemical compound CC(O)C1=CC(N)=CC=C1N HHVMYUPMJJDVPG-UHFFFAOYSA-N 0.000 claims description 4
- KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 claims description 4
- KDBUTNSQYYLYOY-UHFFFAOYSA-N 2-(4,5-diaminopyrazol-1-yl)ethanol Chemical compound NC=1C=NN(CCO)C=1N KDBUTNSQYYLYOY-UHFFFAOYSA-N 0.000 claims description 4
- BYYOWEYWJDNTBJ-UHFFFAOYSA-N 2-[(4-methylphenyl)methyl]pyrazole-3,4-diamine Chemical compound C1=CC(C)=CC=C1CN1C(N)=C(N)C=N1 BYYOWEYWJDNTBJ-UHFFFAOYSA-N 0.000 claims description 4
- HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims description 4
- ALQKEYVDQYGZDN-UHFFFAOYSA-N 2-amino-6-methylphenol Chemical compound CC1=CC=CC(N)=C1O ALQKEYVDQYGZDN-UHFFFAOYSA-N 0.000 claims description 4
- URPJUMVYJFHGOR-UHFFFAOYSA-N 2-benzylpyrazole-3,4-diamine Chemical compound NC1=C(N)C=NN1CC1=CC=CC=C1 URPJUMVYJFHGOR-UHFFFAOYSA-N 0.000 claims description 4
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 4
- QIMMUPPBPVKWKM-UHFFFAOYSA-N 2-methylnaphthalene Chemical compound C1=CC=CC2=CC(C)=CC=C21 QIMMUPPBPVKWKM-UHFFFAOYSA-N 0.000 claims 2
- 238000009903 catalytic hydrogenation reaction Methods 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 239000000543 intermediate Substances 0.000 description 18
- 229920000642 polymer Polymers 0.000 description 13
- 239000000975 dye Substances 0.000 description 10
- 239000002562 thickening agent Substances 0.000 description 10
- 239000002671 adjuvant Substances 0.000 description 9
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 7
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 7
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 7
- 230000003750 conditioning effect Effects 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 238000004040 coloring Methods 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 125000000623 heterocyclic group Chemical group 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- 239000002280 amphoteric surfactant Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 239000003093 cationic surfactant Substances 0.000 description 4
- 239000000982 direct dye Substances 0.000 description 4
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 239000002243 precursor Substances 0.000 description 4
- MGSRCZKZVOBKFT-UHFFFAOYSA-N thymol Chemical compound CC(C)C1=CC=C(C)C=C1O MGSRCZKZVOBKFT-UHFFFAOYSA-N 0.000 description 4
- JDTDIZGWSVNMDX-UHFFFAOYSA-N 1-(5-amino-2-hydroxyphenyl)ethane-1,2-diol Chemical compound NC1=CC=C(O)C(C(O)CO)=C1 JDTDIZGWSVNMDX-UHFFFAOYSA-N 0.000 description 3
- UFBJCMHMOXMLKC-UHFFFAOYSA-N 2,4-dinitrophenol Chemical compound OC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O UFBJCMHMOXMLKC-UHFFFAOYSA-N 0.000 description 3
- XNQXQEPVQJUMCX-UHFFFAOYSA-N 4-[2-(2,4-diaminophenoxy)pyridin-3-yl]oxybenzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OC1=CC=CN=C1OC1=CC=C(N)C=C1N XNQXQEPVQJUMCX-UHFFFAOYSA-N 0.000 description 3
- ITTQLMJTNCLSJJ-UHFFFAOYSA-N 4-[2-(2,4-diaminophenoxy)pyridin-4-yl]oxybenzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OC1=CC=NC(OC=2C(=CC(N)=CC=2)N)=C1 ITTQLMJTNCLSJJ-UHFFFAOYSA-N 0.000 description 3
- DXXCWFLCICIXJC-UHFFFAOYSA-N 4-[6-(2,4-diaminophenoxy)-2-methylpyrimidin-4-yl]oxybenzene-1,3-diamine Chemical compound C=1C(OC=2C(=CC(N)=CC=2)N)=NC(C)=NC=1OC1=CC=C(N)C=C1N DXXCWFLCICIXJC-UHFFFAOYSA-N 0.000 description 3
- TXULDUUXQNHQMM-UHFFFAOYSA-N 4-[6-(2,4-diaminophenoxy)-4-methoxypyridin-2-yl]oxybenzene-1,3-diamine Chemical compound N=1C(OC=2C(=CC(N)=CC=2)N)=CC(OC)=CC=1OC1=CC=C(N)C=C1N TXULDUUXQNHQMM-UHFFFAOYSA-N 0.000 description 3
- CHNPGPWUZRDUCC-UHFFFAOYSA-N 4-[6-(2,4-diaminophenoxy)-5-methoxypyrimidin-4-yl]oxybenzene-1,3-diamine Chemical compound N1=CN=C(OC=2C(=CC(N)=CC=2)N)C(OC)=C1OC1=CC=C(N)C=C1N CHNPGPWUZRDUCC-UHFFFAOYSA-N 0.000 description 3
- ZINAJXDZQUYUSK-UHFFFAOYSA-N 4-[6-(2,4-diaminophenoxy)pyrimidin-4-yl]oxybenzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OC1=CC(OC=2C(=CC(N)=CC=2)N)=NC=N1 ZINAJXDZQUYUSK-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 3
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- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 3
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 3
- 239000000490 cosmetic additive Substances 0.000 description 3
- 229940018564 m-phenylenediamine Drugs 0.000 description 3
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- 150000004989 p-phenylenediamines Chemical class 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
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- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 2
- IYNWDOLJDNUWPD-UHFFFAOYSA-N 1-(2,5-diaminophenyl)ethane-1,2-diol Chemical compound NC1=CC=C(N)C(C(O)CO)=C1 IYNWDOLJDNUWPD-UHFFFAOYSA-N 0.000 description 2
- ORVPXPKEZLTMNW-UHFFFAOYSA-N 1h-indol-7-ol Chemical compound OC1=CC=CC2=C1NC=C2 ORVPXPKEZLTMNW-UHFFFAOYSA-N 0.000 description 2
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- NLMKTBGFQGKQEV-UHFFFAOYSA-N 2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hexadecoxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethanol Chemical compound CCCCCCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO NLMKTBGFQGKQEV-UHFFFAOYSA-N 0.000 description 2
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- 230000002378 acidificating effect Effects 0.000 description 2
- 239000002535 acidifier Substances 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
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- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000008107 starch Chemical class 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- AISMNBXOJRHCIA-UHFFFAOYSA-N trimethylazanium;bromide Chemical compound Br.CN(C)C AISMNBXOJRHCIA-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/62—Oxygen or sulfur atoms
- C07D213/69—Two or more oxygen atoms
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4926—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
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- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
- A61K8/4953—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom containing pyrimidine ring derivatives, e.g. minoxidil
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
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Abstract
用于氧化性染发的染发组合物的偶合剂是式(1)的化合物,其中Y是CH或N,且Z是H、OCH3、NH2和具有1至4个碳原子的烷基,条件是:当Y是N时,2,4-二氨基苯氧基部分位于嘧啶环的4和6位。
Description
发明领域
本发明涉及用于包括一种或多种氧化性染发剂和一种或多种氧化剂的染发组合物中的新的偶合剂。本发明还涉及这些新的偶合剂的染发组合物,以及使用含有这些偶合剂的组合物给头发上色或染色。
发明背景
染发是自古以来应用各种方法实践的操作。在现代,最广泛应用于头发染色的方法是用头发染色体系通过氧化染色过程来使头发着色,该头发染色体系联合使用一种或多种氧化性染发剂与一种或多种氧化剂。
最常见的是,联合使用一种过氧化剂与一种或多种氧化性染发剂,氧化性染发剂一般是小分子,能够扩散到头发中,并且包括一种或多种主要中间体和一种或多种偶合剂。在该方法中,使用过氧化物材料例如过氧化氢来激活小分子的主要中间体,以使它们与偶合剂反应,在发干上形成较大的化合物,从而给头发染上各种色调和颜色。
在此类氧化性染发体系和组合物中已使用了很多种主要中间体和偶合剂。在所使用的主要中间体中,可提及的有对苯二胺、对甲苯二胺、对氨基苯酚、4-氨基-3-甲基苯酚,而可提及的偶合剂有间苯二酚、2-甲基间苯二酚、3-氨基苯酚和5-氨基-2-甲基苯酚。已经用基于对苯二胺的染料产生了多种色调。
为了给头发提供蓝色染色,已经广泛地将间苯二胺与对苯二胺作为主要中间体联合使用。然而,所获得的蓝色染料会发生分子内环化,形成红色的2,8-二氨基吩嗪。这种转化被认为是头发褪色成红色(热磨损或红色褪色)的原因。环化的速度取决于取代基的位置,并且可通过使用具有供电子取代基,例如烷氧基的间苯二胺来降低环化速度。由于经过一段时间后颜色会改变,需要新的蓝色偶合剂用于氧化性染发组合物和系统。
发明概述
本发明提供了新的式(1)的偶合剂:
其中Y选自CH或N,且Z选自H、OCH3、NH2和具有1至4个碳原子的烷基,条件是:当Y是N时,2,4-二氨基苯氧基部分位于嘧啶环的4和6位。
这些新的偶合剂用于给头发提供染料被头发良好地摄取的上色,以及提供在较长的一段时间内保持稳定的色调或颜色。本发明新的偶合剂是用于提供给染发,以赋予头发具有良好的耐洗性、具有良好的选择性并且在暴露于光、汗水或洗发香波时不发生显著改变的颜色或色调。
发明详述
本发明偶合剂化合物是式(1)的化合物
其中Y选自CH或N,且Z选自H、OCH3、NH2和具有1至4个碳原子的烷基,条件是:当Y是N时,2,4-二氨基苯氧基部分位于嘧啶环的4和6位。
优选地,Y是CH或N,且Z是H、OCH3或CH3。
尤其优选的本发明偶合剂是下列化合物:
4-{[2-(2,4-二氨基苯氧基)吡啶-3-基]氧基}苯-1,3-二胺;
4-{[2-(2,4-二氨基苯氧基)吡啶-4-基]氧基}苯-1,3-二胺;
4-{[2-(2,4-二氨基苯氧基)-4-甲氧基-吡啶-6-基]氧基}苯-1,3-二胺;
4-{[6-(2,4-二氨基苯氧基)嘧啶-4-基]氧基}苯-1,3-二胺;
4-{[6-(2,4-二氨基苯氧基)-2-甲基-嘧啶-4-基]氧基}苯-1,3-二胺;和
4-{[6-(2,4-二氨基苯氧基)-5-甲氧基-嘧啶-4-基]氧基}苯-1,3-二胺。
本发明式(1)新的偶合剂化合物易于通过下述反应顺序制得,其中:Y和Z如上所定义;当Y是CH时,W是OH,当Y是N时,W是选自Cl、Br或F的卤素,并且,当Y是N时,R是OH,当Y是CH时,R是选自Cl、Br或F的卤素,条件是:当Y是N时,W在嘧啶环的4和6位。
在该合成中,当Y是CH时,将其中W分别是OH的式(2)化合物与2,4-二硝基-卤代苯、优选2,4-二硝基-氟苯在碳酸钾存在下反应,生成式(3)化合物。用Pd/C在氢气压力下将式(3)化合物氢化,生成其中Y是CH的式(1)的化合物。
在该合成中,当Y是N时,将其中W是连接在嘧啶环的4和6位的卤素的式(2)化合物与2,4-二硝基苯酚反应,生成其中2,4-二硝基苯氧基部分在嘧啶环的4和6位上连接于该嘧啶环的式(3)化合物。用Pd/C在氢气压力下将此式(3)化合物氢化,生成其中Y是N,且2,4-二氨基苯氧基部分在嘧啶环的4和6位上连接于该嘧啶环的式(1)的化合物。
合成实施例1-3
在上述合成中,使用2,4-二硝基-卤代苯与其中W是OH的合适的式(2)的化合物,制得了下列化合物:
4-{[2-(2,4-二氨基苯氧基)吡啶-3-基]氧基}苯-1,3-二胺;
4-{[2-(2,4-二氨基苯氧基)吡啶-4-基]氧基}苯-1,3-二胺;和
4-{[2-(2,4-二氨基苯氧基)-4-甲氧基-吡啶-6-基]氧基}苯-1,3-二胺。
合成实施例4-6
在上述合成中,使用2,4-二硝基苯酚与其中W是连接在嘧啶环的4和6位的Cl的合适的式(2)化合物,制得了下列化合物:
4-{[6-(2,4-二氨基苯氧基)嘧啶-4-基]氧基}苯-1,3-二胺;
4-{[6-(2,4-二氨基苯氧基)-2-甲基-嘧啶-4-基]氧基}苯-1,3-二胺;和
4-{[6-(2,4-二氨基苯氧基)-5-甲氧基-嘧啶-4-基]氧基}苯-1,3-二胺。
本发明所用术语“染发组合物”(在本发明中还称为下述同义词:头发染色组合物、头发上色组合物或染发水)是指在与显色剂组合物混合之前的,含有包括本发明新化合物的氧化性染料的组合物。术语“显色剂组合物”(还称为氧化剂组合物或过氧化物组合物)是指在与染发组合物混合之前的含有一种氧化剂的组合物。可交换使用的术语“染发产品”或“染发体系”(还称为头发染色系统、头发染色产品或头发上色系统)是指在混合之前的染发组合物和显色剂组合物的组合,并且还可以包括调理剂产品和使用说明书,此类产品或系统经常包装为成套用品提供。术语“染发产品组合物”是指通过将染发组合物和显色剂组合物混合而形成的组合物。“载体”(或载体或基质)是指包含在组合物中的,除活性剂(例如染发组合物的氧化性头发染料)外的成分的组合。
本发明染发(即头发染色)组合物可含有与氧化性染料主要中间体组合的本发明新的偶合剂,并且还可以含有其它主要偶合剂。因此,本发明新的偶合剂可以与一种或多种偶合剂和主要中间体联合使用。
合适的已知的主要中间体包括,例如:
对苯二胺衍生物,例如:苯-1,4-二胺(通常称为对苯二胺)、2-甲基-苯-1,4-二胺、2-氯-苯-1,4-二胺、N-苯基-苯-1,4-二胺、N-(2-乙氧基乙基)苯-1,4-二胺、2-[(4-氨基-苯基)-(2-羟基-乙基)-氨基]-乙醇(通常称为N,N-双(2-羟基乙基)-对苯二胺)、(2,5-二氨基-苯基)-甲醇、1-(2,5-二氨基-苯基)-乙醇、2-(2,5-二氨基-苯基)-乙醇、N-(4-氨基苯基)苯-1,4-二胺、2,6-二甲基-苯-1,4-二胺、2-异丙基-苯-1,4-二胺、1-[(4-氨基苯基)氨基]-丙-2-醇、2-丙基-苯-1,4-二胺、1,3-双[(4-氨基苯基)(2-羟基乙基)氨基]丙-2-醇、N4,N4,2-三甲基苯-1,4-二胺、2-甲氧基-苯-1,4-二胺、1-(2,5-二氨基苯基)乙烷-1,2-二醇、2,3-二甲基-苯-1,4-二胺、N-(4-氨基-3-羟基-苯基)-乙酰胺、2,6-二乙基苯-1,4-二胺、2,5-二甲基苯-1,4-二胺、2-噻吩-2-基苯-1,4-二胺、2-噻吩-3-基苯-1,4-二胺、2-吡啶-3-基苯-1,4-二胺、1,1′-联苯-2,5-二胺、2-(甲氧基甲基)苯-1,4-二胺、2-(氨基甲基)苯-1,4-二胺、2-(2,5-二氨基苯氧基)乙醇、N-[2-(2,5-二氨基苯氧基)乙基]-乙酰胺、N,N-二甲基苯-1,4-二胺、N,N-二乙基苯-1,4-二胺、N,N-二丙基苯-1,4-二胺、2-[(4-氨基苯基)(乙基)氨基]乙醇、2-[(4-氨基-3-甲基-苯基)-(2-羟基-乙基)-氨基]-乙醇、N-(2-甲氧基乙基)-苯-1,4-二胺、3-[(4-氨基苯基)氨基]丙烷-1-醇、3-[(4-氨基苯基)-氨基]丙-1,2-二醇、N-{4-[(4-氨基苯基)氨基]丁基}苯-1,4-二胺和2-[2-(2-{2-[(2,5-二氨基苯基)-氧基]乙氧基}乙氧基)乙氧基]苯-1,4-二胺;
对氨基苯酚衍生物,例如:4-氨基-苯酚(通常称为对氨基苯酚)、4-甲基氨基-苯酚、4-氨基-3-甲基-苯酚、4-氨基-2-羟基甲基-苯酚、4-氨基-2-甲基-苯酚、4-氨基-2-[(2-羟基-乙基氨基)-甲基]-苯酚、4-氨基-2-甲氧基甲基-苯酚、5-氨基-2-羟基-苯甲酸、1-(5-氨基-2-羟基-苯基)-乙烷-1,2-二醇、4-氨基-2-(2-羟基-乙基)-苯酚、4-氨基-3-(羟基甲基)苯酚、4-氨基-3-氟-苯酚、4-氨基-2-(氨基甲基)-苯酚和4-氨基-2-氟-苯酚;
邻氨基苯酚衍生物,例如:2-氨基-苯酚(通常称为邻氨基苯酚)、2,4-二氨基苯酚、2-氨基-5-甲基-苯酚、2-氨基-6-甲基-苯酚、N-(4-氨基-3-羟基-苯基)-乙酰胺和2-氨基-4-甲基-苯酚;和
杂环衍生物,例如:嘧啶-2,4,5,6-四胺(通常称为2,4,5,6-四氨基吡啶)、1-甲基-1H-吡唑-4,5-二胺、2-(4,5-二氨基-1H-吡唑-1-基)乙醇、N2,N2-二甲基-吡啶-2,5-二胺、2-[(3-氨基-6-甲氧基吡啶-2-基)氨基]乙醇、6-甲氧基-N2-甲基-吡啶-2,3-二胺、2,5,6-三氨基嘧啶-4(1H)-酮、吡啶-2,5-二胺、1-异丙基-1H-吡唑-4,5-二胺、1-(4-甲基苄基)-1H-吡唑-4,5-二胺、1-(苄基)-1H-吡唑-4,5-二胺和1-(4-氯苄基)-1H-吡唑-4,5-二胺。
本发明新的式(1)偶合剂可以与任意合适的偶合剂一起用于本发明染发组合物或系统中。
合适的已知的偶合剂包括,例如:
苯酚、间苯二酚和萘酚衍生物,例如:萘-1,7-二酚、苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、萘-1,5-二酚、萘-2,7-二酚、苯-1,4-二酚、2-甲基-苯-1,3-二酚、7-氨基-4-羟基-萘-2-磺酸、2-异丙基-5-甲基苯酚、1,2,3,4-四氢萘-1,5-二酚、2-氯-苯-1,3-二酚、4-羟基-萘-1-磺酸、苯-1,2,3-三酚、萘-2,3-二酚、5-二氯-2-甲基苯-1,3-二酚、4,6-二氯苯-1,3-二酚和2,3-二羟基-[1,4]萘醌;
间苯二胺类,例如:2,4-二氨基苯酚、苯-1,3-二胺、2-(2,4-二氨基-苯氧基)-乙醇、2-[(3-氨基-苯基)-(2-羟基-乙基)-氨基]-乙醇、2-甲基-苯-1,3-二胺、2-[[2-(2,4-二氨基-苯氧基)-乙基]-(2-羟基-乙基)-氨基]-乙醇、4-{3-[(2,4-二氨基苯基)氧基]丙氧基}苯-1,3-二胺、2-(2,4-二氨基-苯基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、4-(2-氨基-乙氧基)-苯-1,3-二胺、(2,4-二氨基-苯氧基)-乙酸、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇、4-乙氧基-6-甲基-苯-1,3-二胺、2-(2,4-二氨基-5-甲基-苯氧基)-乙醇、4,6-二甲氧基-苯-1,3-二胺、2-[3-(2-羟基-乙基氨基)-2-甲基-苯基氨基]-乙醇、3-(2,4-二氨基-苯氧基)-丙烷-1-醇、N-[3-(二甲基氨基)苯基]脲、4-甲氧基-6-甲基苯-1,3-二胺、4-氟-6-甲基苯-1,3-二胺、2-({3-[(2-羟基乙基)氨基]-4,6-二甲氧基苯基}-氨基)乙醇、3-(2,4-二氨基苯氧基)-丙-1,2-二醇、2-[2-氨基-4-(甲基氨基)-苯氧基]乙醇、2-[(5-氨基-2-乙氧基-苯基)-(2-羟基-乙基)-氨基]-乙醇、2-[(3-氨基苯基)氨基]乙醇、N-(2-氨基乙基)苯-1,3-二胺、4-{[(2,4-二氨基-苯基)氧基]甲氧基}-苯-1,3-二胺和2,4-二甲氧基苯-1,3-二胺;
间氨基苯酚类,例如:3-氨基-苯酚、2-(3-羟基-4-甲基-苯基氨基)-乙酰胺、2-(3-羟基-苯基氨基)-乙酰胺、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、5-氨基-2,4-二氯-苯酚、3-氨基-2-甲基-苯酚、3-氨基-2-氯-6-甲基-苯酚、5-氨基-2-(2-羟基-乙氧基)-苯酚、2-氯-5-(2,2,2-三氟-乙基氨基)-苯酚、5-氨基-4-氯-2-甲基-苯酚、3-环戊基氨基-苯酚、5-[(2-羟基乙基)氨基]-4-甲氧基-2-甲基苯酚、5-氨基-4-甲氧基-2-甲基苯酚、3-(二甲基氨基)苯酚、3-(二乙基氨基)苯酚、5-氨基-4-氟-2-甲基苯酚、5-氨基-4-乙氧基-2-甲基苯酚、3-氨基-2,4-二氯-苯酚、3-[(2-甲氧基乙基)氨基]苯酚、3-[(2-羟基乙基)氨基]苯酚、5-氨基-2-乙基-苯酚、5-氨基-2-甲氧基苯酚、5-[(3-羟基丙基)氨基]-2-甲基苯酚、3-[(3-羟基-2-甲基苯基)-氨基]丙-1,2-二醇和3-[(2-羟基乙基)氨基]-2-甲基苯酚;和
杂环衍生物,例如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、6-甲氧基喹啉-8-胺、4-甲基吡啶-2,6-二酚、2,3-二氢-1,4-苯并二氧杂环己烯-5-醇、1,3-苯并二氧杂环戊烯-5-醇、2-(1,3-苯并二氧杂环戊烯-5-基氨基)乙醇、3,4-二甲基吡啶-2,6-二酚、5-氯吡啶-2,3-二酚、2,6-二甲氧基吡啶-3,5-二胺、1,3-苯并二氧杂环戊烯-5-胺、2-{[3,5-二氨基-6-(2-羟基-乙氧基)-吡啶-2-基]氧基}-乙醇、1H-吲哚-4-酚、5-氨基-2,6-二甲氧基吡啶-3-酚、1H-吲哚-5,6-二酚、1H-吲哚-7-酚、1H-吲哚-5-酚、1H-吲哚-6-酚、6-溴-1,3-苯并二氧杂环戊烯-5-醇、2-氨基吡啶-3-酚、吡啶-2,6-二胺、3-[(3,5-二氨基吡啶-2-基)氧基]丙-1,2-二醇、5-[(3,5-二氨基吡啶-2-基)氧基]戊-1,3-二醇、1H-吲哚-2,3-二酮、二氢吲哚-5,6-二酚、3,5-二甲氧基吡啶-2,6-二胺、6-甲氧基吡啶-2,3-二胺和3,4-二氢-2H-1,4-苯并噁嗪-6-胺。
优选的主要中间体包括:
对苯二胺衍生物,例如:2-甲基-苯-1,4-二胺、苯-1,4-二胺、1-(2,5-二氨基-苯基)-乙醇、2-(2,5-二氨基-苯基)-乙醇、N-(2-甲氧基乙基)苯-1,4-二胺、2-[(4-氨基-苯基)-(2-羟基-乙基)-氨基]-乙醇和1-(2,5-二氨基苯基)乙烷-1,2-二醇;
对氨基苯酚衍生物,例如4-氨基-苯酚、4-甲基氨基-苯酚、4-氨基-3-甲基-苯酚、4-氨基-2-甲氧基甲基-苯酚和1-(5-氨基-2-羟基-苯基)-乙烷-1,2-二醇;
邻氨基苯酚衍生物,例如:2-氨基-苯酚、2-氨基-5-甲基-苯酚、2-氨基-6-甲基-苯酚、N-(4-氨基-3-羟基-苯基)-乙酰胺和2-氨基-4-甲基-苯酚;和
杂环衍生物,例如:嘧啶-2,4,5,6-四胺、1-甲基-1 H-吡唑-4,5-二胺、2-(4,5-二氨基-1H-吡唑-1-基)乙醇、1-(4-甲基苄基)-1H-吡唑-4,5-二胺、1-(苄基)-1H-吡唑-4,5-二胺和N2,N2-二甲基-吡啶-2,5-二胺。
优选的偶合剂包括:
苯酚、间苯二酚和萘酚衍生物,例如:萘-1,7-二酚、苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、萘-1,5-二酚、萘-2,7-二酚、苯-1,4-二酚、2-甲基-苯-1,3-二酚和2-异丙基-5-甲基苯酚;
间苯二胺类,例如:苯-1,3-二胺、2-(2,4-二氨基-苯氧基)-乙醇、4-{3-[(2,4-二氨基苯基)氧基]丙氧基}苯-1,3-二胺、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇;
间氨基苯酚类,例如:3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚和3-氨基-2-甲基-苯酚;和
杂环衍生物,例如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1,3-苯并二氧杂环戊烯-5-醇、1,3-苯并二氧杂环戊烯-5-胺、1H-吲哚-4-酚、1H-吲哚-5,6-二酚、1H-吲哚-7-酚、1H-吲哚-5-酚、1H-吲哚-6-酚、1H-吲哚-2,3-二酮、吡啶-2,6-二胺和2-氨基吡啶-3-酚。
最优选的主要中间体包括:
对苯二胺衍生物,例如:2-甲基-苯-1,4-二胺、苯-1,4-二胺、2-(2,5-二氨基-苯基)-乙醇、1-(2,5-二氨基-苯基)-乙醇和2-[(4-氨基-苯基)-(2-羟基-乙基)-氨基]-乙醇;
对氨基苯酚衍生物,例如:4-氨基-苯酚、4-甲基氨基-苯酚、4-氨基-3-甲基-苯酚和1-(5-氨基-2-羟基-苯基)-乙烷-1,2-二醇;
邻氨基苯酚类,例如:2-氨基-苯酚、2-氨基-5-甲基-苯酚、2-氨基-6-甲基-苯酚和N-(4-氨基-3-羟基-苯基)-乙酰胺;和
杂环衍生物,例如:嘧啶-2,4,5,6-四胺、2-(4,5-二氨基-1H-吡唑-1-基)乙醇、1-(4-甲基苄基)-1H-吡唑-4,5-二胺和1-(苄基)-1H-吡唑-4,5-二胺。
最优选的偶合剂包括:
苯酚、间苯二酚和萘酚衍生物,例如:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚和2-甲基-苯-1,3-二酚;
间苯二胺,例如:2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇;
间氨基苯酚类,例如:3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚和3-氨基-2-甲基-苯酚;和
杂环衍生物,例如:3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
可以理解,对于偶合剂化合物和主要中间体化合物,包括本发明的新化合物,当它们是碱时,其可以以游离碱的形式使用,或者以其与有机酸或无机酸,例如盐酸、柠檬酸、乙酸、酒石酸或硫酸形成的生理相容性盐的形式使用,或者当它们具有芳族OH基时,可以以与碱形成的盐,例如碱金属的酚盐形式使用。
染料前体(例如主要中间体和偶合剂化合物,包括本发明的新化合物)在本发明染发组合物中的总量一般为染发组合物总重量的约0.002%至约20%、优选约0.04%至约10%、最优选约0.1%至约7.0%。主要中间体与偶合剂化合物一般以等摩尔量使用。然而,可使用过量或不足量的主要中间体,即主要中间体与偶合剂的摩尔比一般为约5∶1至约1∶5。
本发明染发组合物含有有效染发量的本发明偶合剂,其量一般为染发组合物重量的约0.001%至约10%、优选约0.01%至约5.0%。当存在其它偶合剂时,其典型地以这样的量存在,使得偶合剂在本发明组合物中的总浓度为约0.002%至约10%重量百分比、优选约0.01%至约5.0%重量百分比。主要中间体以有效染发浓度存在,其含量一般为染发组合物重量的约0.001%至约10.0%重量百分比、优选约0.01%至约5.0%重量百分比。染发组合物的其余部分包含偶合剂和主要中间体的载体或赋形剂,并包括如下所述的各种辅剂。
可使用任意合适的载体或赋形剂,通常为水溶液或水醇溶液,优选水溶液。载体或赋形剂一般占染发组合物重量的80%以上、典型地为90%至99%重量百分比、优选94%至99%重量百分比。本发明染发组合物可含有一种或多种下列物质作为辅剂:阳离子表面活性剂、阴离子表面活性剂、两性表面活性剂或两性离子表面活性剂,香料,抗氧化剂例如抗坏血酸、巯基乙酸或亚硫酸钠,螯合剂例如EDTA,增稠剂,碱化剂或酸化剂,溶剂,稀释剂,惰性物质,分散剂,渗透剂,消泡剂,酶和其它染料剂(例如合成的直接染料和天然染料)。这些辅剂是常用于染发组合物中的化妆品添加成分。
本发明染发组合物通过与合适的氧化剂混合来使用,其中氧化剂与染发前体反应以使头发染料显色。在本发明染发产品组合物中可使用任意合适的氧化剂,尤其是过氧化氢(H2O2)或其前体。过氧化脲,碱金属的过硫酸盐、过硼酸盐和过碳酸盐,尤其是钠盐,和三聚氰胺过氧化物也是合适的。氧化剂通常是在一般称为显色剂组合物的含水组合物中提供,显色剂组合物通常是作为染发成品的单独组分提供,并且放在一个单独的容器中。显色剂组合物还可以在相容程度上含有用于形成显色剂组合物所需的各种成分,即过氧化物稳定剂、泡沫形成剂等,并且可掺入一种或多种上述辅剂,例如表面活性剂、增稠剂、pH调节剂等。经过将染发组合物与显色组合物混合以形成染发产品组合物,当把组合物施用到头发上时,在染发产品组合物中提供辅剂以实现所需的产品性质例如pH、粘度、流变学特征等。
依据本发明,染发产品组合物的形式可以是,例如溶液,尤其是水溶液或水-醇溶液。然而,优选的形式是粘稠液体、霜膏、凝胶或乳液,其组成是染料成分与适于特定制剂的常规化妆品添加成分的混合物。
下面描述了用于染发组合物和显色剂组合物的,及因此在本发明染发产品组合物中的合适的常规化妆品添加成分,并且可以使用它们来获得染发组合物、显色剂组合物和染发产品组合物所需的特征。
溶剂:除了水以外,可使用的溶剂还有低级链烷醇(例如乙醇、丙醇、异丙醇、苯甲醇);多元醇(例如卡必醇、丙二醇、己二醇、甘油)。参见WO98/27941(关于稀释剂的部分),该文件引入本文以供参考。还参见美国专利6027538,该文件引入本文以供参考。在合适的处理下,高级醇例如C8至C1 8脂肪醇,尤其是鲸蜡醇是合适的有机溶剂,条件是在掺入其它的,通常是亲脂性材料之前,首先将其通过熔化液化,典型地在低温(50℃至80℃)下熔化液化。
典型地,有机溶剂以占染发组合物重量约5%至约30%的量存在于染发组合物中。水通常以占染发组合物重量的约5%至约90%、优选约15%至约75%、最优选约30%至约65%的量存在。
表面活性剂:这些原料选自下列种类:阴离子表面活性剂、阳离子表面活性剂、两性表面活性剂(包括两性离子表面活性剂)或非离子表面活性剂化合物。(下文单独描述通常作为头发调理剂被包括在内的阳离子表面活性剂) 除阳离子表面活性剂之外,合适的表面活性剂包括脂肪醇硫酸盐、乙氧基化脂肪醇硫酸盐、烷基磺酸盐、烷基苯磺酸盐、烷基三甲基铵盐、烷基甜菜碱、乙氧基化脂肪醇、乙氧基化脂肪酸、乙氧基化烷基苯酚、乙二醇和/或丙二醇的嵌段聚合物、甘油酯、磷酸酯、脂肪酸链烷醇酰胺和乙氧基化脂肪酸酯、烷基硫酸盐、乙氧基化烷基硫酸盐、烷基甘油基醚磺酸盐、甲基酰基牛磺酸盐、酰基羟乙基磺酸盐、烷基乙氧基羧酸盐、脂肪酸一乙醇酰胺和脂肪酸二乙醇酰胺。尤其有用的是烷基硫酸钠和铵,具有1至3个氧化乙烯基的醚硫酸钠和醚硫酸铵,以及作为Tergitols,例如C11-C15Pareth-9,和Neodols,例如C12-C15 Pareth-3销售的非离子表面活性剂。包括它们是出于各种原因,例如为了促进增稠、用于形成乳液、为了在施用染发产品组合物期间帮助润湿头发等。两性表面活性剂,包括例如具有约10至约20个碳原子的烷基或烷基酰氨基的天冬酰胺衍生物以及甜菜碱、磺基甜菜碱、甘氨酸盐和丙酸盐。适用于本发明的典型的两性表面活性剂包括月桂基甜菜碱、月桂酰基两性甘氨酸盐、月桂酰基两性丙酸盐、月桂基磺基甜菜碱、肉豆蔻酰氨基丙基甜菜碱、十四烷基甜菜碱、硬脂酰基两性丙基磺酸盐、椰油酰氨基乙基甜菜碱、椰油酰氨基丙基甜菜碱、椰油基两性甘氨酸盐、椰油基两性羧基丙酸盐、椰油基两性羧基甘氨酸盐、椰油基甜菜碱和椰油基两性丙酸盐。参考公布于1998年11月26日的WO 98/52523和公布于2001年8月30日的WO 01/62221,这两个文件都引入本文以供参考。
表面活性剂在染发组合物中的量,以重量计,通常为约0.1%至30%、优选为1%至15%。
增稠剂:合适的增稠剂包括例如高级脂肪醇、淀粉、纤维素衍生物、凡士林、石蜡油、脂肪酸和基于聚丙烯酸和聚氨酯聚合物的阴离子和非离子聚合增稠剂。实例有羟乙基纤维素、羟甲基纤维素和其它纤维素衍生物,疏水改性的阴离子聚合物和非离子聚合物,尤其是既具有亲水部分又具有疏水部分的聚合物(即两亲聚合物)。有用的非离子聚合物包括聚氨酯衍生物例如PEG-150/硬脂醇/SDMI共聚物。合适的聚醚尿烷是由Rohm & Haas销售的Aculyn22、44和Aculyn46聚合物。其它有用的两亲聚合物公开于美国专利6010541,该文件引入本文以供参考。还参见上述WO 01/62221。可用作增稠剂的阴离子聚合物的实例是丙烯酸酯共聚物、丙烯酸酯/十六烷基聚氧乙烯醚-20异丁烯酸酯共聚物、丙烯酸酯/十六烷基聚氧乙烯醚-20衣康酸酯共聚物和丙烯酸酯/二十二烷基聚氧乙烯醚-25丙烯酸酯共聚物。对于缔合型增稠剂例如Aculyns 22、44和46,聚合物可包含在染发产品的染发组合物和显色剂组合物当中的一个组合物中,表面活性剂包含在另一个组合物中。因此,通过将染发组合物与显色剂组合物混合,获得了必需的粘度。增稠剂以一定量提供,以使产品施用到头发上时具有适当的粘稠度。这样的产品一般具有1000至100000cps的粘度,并且经常具有触变流体学性质。
pH调节剂:用于调节本发明染发组合物的pH的合适的材料包括碱化剂,例如碱金属和铵的氢氧化物和碳酸盐,尤其是氢氧化钠和碳酸铵,氨,有机胺,包括甲基乙醇胺、氨基甲基丙醇、一乙醇胺、二乙醇胺和三乙醇胺,和酸化剂,例如无机酸和有机酸,例如磷酸、乙酸、抗坏血酸、柠檬酸或酒石酸、盐酸等。参见美国专利6027538,该文件引入本文以供参考。
调理剂:合适的材料包括聚硅氧烷和聚硅氧烷衍生物;烃油;单季化合物和季铵化的聚合物。典型地,单季化合物是阳离子化合物,但是也可包括提供调理效果的甜菜碱和其它两性以及两性离子物质。合适的单季化合物包括二十二烷基三烷基氯化铵、二十二烷基三甲基氯化铵、烷基苄基二甲基溴化铵或烷基苄基二甲基氯化铵、苄基三乙基氯化铵、二(羟基乙基)牛油基甲基氯化铵、C12-18二烷基二甲基氯化铵、十六烷基二甲基氯化铵、鲸蜡硬脂基三甲基溴化铵和鲸蜡硬脂基三甲基氯化铵、十六烷基三甲基溴化铵、十六烷基三甲基氯化铵和十六烷基三甲基硫酸甲酯铵、氯化十六烷基吡啶、椰油酰氨基丙基乙基二甲基硫酸乙酯铵、椰油酰氨基丙基硫酸乙酯、椰油基乙基二甲基硫酸乙酯铵、椰油基三甲基氯化铵和椰油基三甲基硫酸乙酯铵、双二十二烷基二甲基氯化铵、二鲸蜡基二甲基氯化铵、二椰油基二甲基氯化铵、二月桂基二甲基氯化铵、二大豆二甲基氯化铵、二牛油基二甲基氯化铵、氢化牛油基三甲基氯化铵、羟基乙基鲸蜡基二甲基氯化铵、十四烷基二甲基苄基氯化铵、油基二甲基苄基氯化铵、大豆乙氧基甲基硫酸乙酯铵盐、大豆三甲基氯化铵、硬脂基二甲基苄基氯化铵和多种其它化合物。参见WO 98/27941,该文件引入本文以供参考。典型地,季铵化聚合物是阳离子聚合物,但是也可以包括两性和两性离子聚合物。有用的聚合物的实例是聚季铵-4、聚季铵-6、聚季铵-7、聚季铵-8、聚季铵-9、聚季铵-10、聚季铵-22、聚季铵-32、聚季铵-39、聚季铵-44和聚季铵-47。适于调理头发的聚硅氧烷是聚二甲基硅氧烷、氨基封端的聚二甲基硅氧烷、聚二甲基硅氧烷共聚醇和聚二甲基硅氧烷醇。还参见公布于1999年7月15日的WO 99/34770中关于合适的聚硅氧烷的部分,该文件引入本文以供参考。合适的烃油包括矿物油。
调理剂在本发明染发组合物中的含量通常为组合物重量的约0.01%至约5%。
直接染料:依据本发明,染发组合物还可含有相容的直接染料,包括分散黑9、HC黄2、HC黄4、HC黄15、4-硝基邻苯二胺、2-氨基-6-氯-4-硝基苯酚、HC红3、分散紫1、HC蓝2、分散蓝3和分散蓝377。这些直接染料在本发明染发组合物中的含量可以为约0.05%至4.0%重量百分比。
天然成分:例如蛋白质和蛋白质衍生物,以及植物材料例如芦荟、春黄菊和指甲花的提取物。
其它辅剂包括多糖、烷基多苷、缓冲剂、螯合剂、抗氧化剂和如WO01/62221中所述的过氧化物稳定剂等。
上文提及但是没有具体描述的合适的辅剂列在The Cosmetics,Toiletry,and Fragrance Association出版的,International Cosmetics Ingredient Dictionaryand Handbook,(第8版)中,其引入本文以供参考。特别参考Volume 2,Section3(Chemical Classes)和Section 4(Functions),其可用于确定具体的辅剂以实现一个或多个特定目的。
上述常规化妆品成分以适于其功能目的的量使用。例如,用作润湿剂、缔合剂和乳化剂的表面活性剂,一般以约0.1%至30%重量百分比的浓度存在,增稠剂以约0.1%至25%重量百分比的量使用,护发物质典型地以约0.01%至5.0%重量百分比的浓度使用。
当染发产品组合物施用到头发上时,即依据本发明,将染发组合物与显色剂混合之后,根据其组成,染发产品组合物可呈弱酸性、中性或碱性。染发组合物的pH值可以为约6至11.5、优选为约6.8至约10、且尤其为约8至约10。典型地,显色剂组合物的pH为酸性,且其pH一般为约2.5至约6.5、通常为约3至5。可使用如上所述的pH调节剂来调节染发组合物和显色剂组合物的pH。
为了使用染发组合物给头发染发,在临使用前将上述本发明染发组合物与氧化剂混合,并根据头发的量,将足量的该混合物施用到头发上,用量一般为约60克至200克。根据成分的性质、可能的相互作用等,上文列出的某些辅剂(例如增稠剂、调理剂等)可在染发组合物或显色剂组合物,或同时在二者中提供,这是本领域所公知的。
典型地,过氧化氢或其与脲、三聚氰胺、硼酸钠或碳酸钠的加成化合物可以以3%至12%、优选6%的水溶液形式,作为使头发染料显色的氧化剂使用。氧还可以作为氧化剂使用。如果使用6%的过氧化氢溶液作为氧化剂,染发组合物与显色剂组合物的重量比为5∶1至1∶5、但优选1∶1。一般情况下,制备包括主要中间体和偶合剂,包括至少一种式(1)的化合物的染发组合物,然后在使用时,将其与包含在显色剂组合物中的氧化剂,例如H2O2混合,直至获得基本上均匀的组合物,制备后不久将其施加到待染色的头发上,并让其与头发保持接触染发有效长度的时间。让氧化剂与本发明染发组合物的混合物(即染发产品组合物)在头发上于约15℃至50℃下,作用约2分钟至约60分钟、优选约15分钟至45分钟、尤其是约30分钟,用水漂洗头发,并干燥。如果需要,用香波洗涤头发,并漂洗,例如用水或弱酸性溶液例如柠檬酸或酒石酸溶液漂洗。然后将头发干燥。任选,可提供单独的调理产品。
包括染发偶合剂(1)的本发明染发组合物与包括氧化剂的显色剂组合物一起形成用于染发的系统。该系统可作为一个成套用具提供,其在一个包装中包括染发组合物、显色剂、可选择的调理剂或其它滋发产品的单独容器以及使用说明。
尤其有用的本发明式(1)偶合剂将提供具有杰出的染色牢度,尤其是耐光性、耐洗性和耐摩擦性的染发组合物。
染发实施例1
表1所示的下述组合物可用于给Piedmont头发染色。将100g该染发组合物与100g 20体积的过氧化氢混合。将所得混合物施用到头发上,并让其与头发保持接触30分钟。然后用香波洗涤所染色的头发,用水漂洗,并干燥。表1所列出的成分的范围是在染发产品中所列出的物质的示例性有用浓度。
表1
染发组合物
成分 | 范围(wt%) | 重量(%) |
椰油酰氨基丙基甜菜碱聚季铵-22一乙醇胺1油酸柠檬酸28%氢氧化铵1二十二烷基三甲基氯化铵亚硫酸钠EDTA赤藻糖酸乙氧基二甘醇C11-15 Pareth-9(Tergitol15-S-9)C12-15 Pareth-3(Neodol 25-3)异丙醇丙二醇对苯二胺2N,N-双(羟基乙基)-对苯二胺23-甲基-对氨基苯酚2对氨基苯酚2本发明偶合剂5-氨基-2-甲基苯酚2,4-二氨基苯氧基乙醇间苯二胺水 | 0-250-70-152-220-30-151-50-10-10-11-100.5-50.25-52-101-120-50-50-50-50.5-50-50-50-5适量至100.00 | 17.005.002.000.750.105.000.500.100.100.403.501.000.504.002.002mmol2mmol2mmol1mmol4mmol1mmol1mmol1mmol适量至100.00 |
1在该聚集体中,这些成分为2%至15%重量百分比范围内。
2典型地存在这些染料前体当中的至少一种。
使用本发明式(1)偶合剂化合物的染发组分的示例性组合如表A至H中的组合C1至C138所示。参见表A至H中的栏,X代表可依据本发明配制的染料组合。例如,在表A第4栏的第C1号组合中,可将本发明式(1)偶合剂化合物(表A的第1行)与2-甲基-苯-1,4-二胺和2-氨基-苯酚组合,其中Y和Z如上所定义。在表1和表A至H的组合中,尤其优选的式(1)偶合剂化合物如下:
4-{[2-(2,4-二氨基苯氧基)吡啶-3-基]氧基}苯-1,3-二胺;
4-{[2-(2,4-二氨基苯氧基)吡啶-4-基]氧基}苯-1,3-二胺;
4-{[2-(2,4-二氨基苯氧基)-4-甲氧基-吡啶-6-基]氧基}苯-1,3-二胺;
4-{[6-(2,4-二氨基苯氧基)嘧啶-4-基]氧基}苯-1,3-二胺;
4-{[6-(2,4-二氨基苯氧基)-2-甲基-嘧啶-4-基]氧基}苯-1,3-二胺;和
4-{[6-(2,4-二氨基苯氧基)-5-甲氧基-嘧啶-4-基]氧基}苯-1,3-二胺。
通过前面对本发明的描述,本领域的技术人员将领会到,在不背离本发明精神的条件下,可以对其进行修改。因此,本发明的范围不限于具体实施方案举例说明和描述的内容。
Claims (26)
2.如权利要求1所述的化合物,其中Y是CH。
3.如权利要求2所述的化合物,其中Z是H或OCH3。
4.如权利要求1所述的化合物,其中Y是N。
5.如权利要求4所述的化合物,其中Z是H、CH3或OCH3。
6.如权利要求5所述的化合物,其中Z取代基位于嘧啶环的2或5位。
8.如权利要求7所述的方法,其中Y是CH。
9.如权利要求7所述的方法,其中Y是N。
10.如权利要求7所述的方法,其中Z是H、CH3或OCH3。
12.如权利要求11所述的染发产品,其中所述染发组合物还含有一种选自下列物质的偶合剂:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、2-甲基-苯-1,3-二酚、2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇、3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、3-氨基-2-甲基-苯酚、3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
13.如权利要求11所述的染发产品,其中所述主要中间体选自:2-甲基-苯-1,4-二胺、苯-1,4-二胺、2-(2,5-二氨基-苯基)-乙醇、1-(2,5-二氨基-苯基)-乙醇、2-[(4-氨基-苯基)-(2-羟基-乙基)-氨基]-乙醇、4-氨基-苯酚、4-甲基氨基-苯酚、4-氨基-3-甲基-苯酚、1-(5-氨基-2-羟基-苯基)-乙烷-1,2-二醇、2-氨基-苯酚、2-氨基-5-甲基-苯酚、2-氨基-6-甲基-苯酚、N-(4-氨基-3-羟基-苯基)-乙酰胺、嘧啶-2,4,5,6-四胺、2-(4,5-二氨基-1H-吡唑-1-基)乙醇、1-(4-甲基苄基)-1H-吡唑-4,5-二胺和1-(苄基)-1H-吡唑-4,5-二胺。
14.如权利要求13所述的染发产品,其中所述染发组合物还含有选自下列物质的偶合剂:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、2-甲基-苯-1,3-二酚、2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇、3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、3-氨基-2-甲基-苯酚、3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
15.如权利要求11所述的染发产品,其中Z是H、CH3或OCH3。
17.如权利要求16所述的系统,其中Z是H、CH3或OCH3。
19.如权利要求18所述的染发组合物,其中所述染发组合物还含有至少一种选自下列物质的偶合剂:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、2-甲基-苯-1,3-二酚、2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇、3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、3-氨基-2-甲基-苯酚、3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
20.如权利要求18所述的染发组合物,其中所述至少一种主要中间体选自:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-萘-1-酚、2-甲基-苯-1,3-二酚、2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇、3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、3-氨基-2-甲基-苯酚、3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
21.如权利要求20所述的染发组合物,其中所述组合物还包括选自下列物质的偶合剂:苯-1,3-二酚、4-氯苯-1,3-二酚、萘-1-酚、2-甲基-奈1-酚、2-甲基-苯-1,3-二酚、2-(2,4-二氨基-苯氧基)-乙醇、2-(3-氨基-4-甲氧基-苯基氨基)-乙醇、2-[2,4-二氨基-5-(2-羟基-乙氧基)-苯氧基]-乙醇和3-(2,4-二氨基-苯氧基)-丙烷-1-醇、3-氨基-苯酚、5-氨基-2-甲基-苯酚、5-(2-羟基-乙基氨基)-2-甲基-苯酚、3-氨基-2-甲基-苯酚、3,4-二氢-2H-1,4-苯并噁嗪-6-酚、4-甲基-2-苯基-2,4-二氢-3H-吡唑-3-酮、1H-吲哚-6-酚和2-氨基吡啶-3-酚。
22.如权利要求18所述的染发组合物,其中Z是H、CH3或OCH3。
23.如权利要求22所述的染发组合物,其中Y是CH,且Z是H。
24.如权利要求22所述的染发组合物,其中Y是N,且Z是H。
25.染发方法,该方法包括通过将显色剂组合物与如权利要求18所述的染发组合物混合,以形成染发产品组合物,将染发有效量的染发产品组合物施用到头发上,让染发产品组合物与头发接触有效染发的时间段,然后将染发产品组合物从头发上除去。
26.如权利要求25所述的方法,其中Z是H、CH3或OCH3。
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US60/265,295 | 2001-01-31 |
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US (1) | US6693196B2 (zh) |
EP (1) | EP1357889B1 (zh) |
JP (1) | JP2004517936A (zh) |
CN (1) | CN1486170A (zh) |
AT (1) | ATE322246T1 (zh) |
AU (1) | AU2002235431B2 (zh) |
CA (1) | CA2434843C (zh) |
DE (1) | DE60210418T2 (zh) |
ES (1) | ES2261628T3 (zh) |
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US7550499B2 (en) * | 2004-05-12 | 2009-06-23 | Bristol-Myers Squibb Company | Urea antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
EP1954696B1 (en) * | 2005-01-19 | 2011-02-23 | Bristol-Myers Squibb Company | 2-phenoxy-n-(1,3,4-thiadizol-2-yl)pyridin-3-amine derivatives and related compounds as p2y1 receptor inhibitors for the treatment of thromboembolic disorders |
EP1896466B1 (en) * | 2005-06-27 | 2011-04-13 | Bristol-Myers Squibb Company | N-linked heterocyclic antagonists of p2y1 receptor useful in the treatment of thrombotic conditions |
US7700620B2 (en) * | 2005-06-27 | 2010-04-20 | Bristol-Myers Squibb Company | C-linked cyclic antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
US7714002B2 (en) * | 2005-06-27 | 2010-05-11 | Bristol-Myers Squibb Company | Carbocycle and heterocycle antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
ES2360818T3 (es) | 2005-06-27 | 2011-06-09 | Bristol-Myers Squibb Company | Miméticos de urea lineal antagonistas del receptor p2y, útiles en el tratamiento de afecciones trombóticas. |
US7960569B2 (en) * | 2006-10-17 | 2011-06-14 | Bristol-Myers Squibb Company | Indole antagonists of P2Y1 receptor useful in the treatment of thrombotic conditions |
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US3673026A (en) * | 1970-01-12 | 1972-06-27 | Int Paper Co | Method for the manufacture of laminated fabrics |
LU86905A1 (fr) * | 1987-05-29 | 1989-01-19 | Oreal | Nouvelles metaphenylenediamines,leur procede de preparation,composes intermediaires et utilisation de ces metaphenylenediamines en tant que coupleurs pour la teinture d'oxydation des fibres keratiniques et en particulier des cheveux humains |
FR2649887B1 (fr) * | 1989-07-21 | 1994-07-08 | Oreal | Procede de coloration mettant en oeuvre des colorants indoliques et des precurseurs de colorants d'oxydation et agents de teinture mis en oeuvre |
JP4467662B2 (ja) | 1998-12-28 | 2010-05-26 | 三井化学株式会社 | 耐熱性接着剤 |
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MXPA03006832A (es) | 2003-11-13 |
CA2434843A1 (en) | 2002-08-08 |
CA2434843C (en) | 2009-05-26 |
ATE322246T1 (de) | 2006-04-15 |
EP1357889A4 (en) | 2004-12-01 |
US20030061667A1 (en) | 2003-04-03 |
DE60210418T2 (de) | 2006-11-16 |
ES2261628T3 (es) | 2006-11-16 |
EP1357889B1 (en) | 2006-04-05 |
WO2002060400A1 (en) | 2002-08-08 |
DE60210418D1 (de) | 2006-05-18 |
US6693196B2 (en) | 2004-02-17 |
AU2002235431B2 (en) | 2005-04-14 |
JP2004517936A (ja) | 2004-06-17 |
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