JP2003510359A5 - - Google Patents
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- JP2003510359A5 JP2003510359A5 JP2001527795A JP2001527795A JP2003510359A5 JP 2003510359 A5 JP2003510359 A5 JP 2003510359A5 JP 2001527795 A JP2001527795 A JP 2001527795A JP 2001527795 A JP2001527795 A JP 2001527795A JP 2003510359 A5 JP2003510359 A5 JP 2003510359A5
- Authority
- JP
- Japan
- Prior art keywords
- anilino
- triazole
- methyl
- benzylthio
- ylthio
- 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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- 150000001875 compounds Chemical class 0.000 description 29
- -1 4-methyl-anilino Chemical group 0.000 description 11
- 150000003839 salts Chemical class 0.000 description 7
- 239000012453 solvate Substances 0.000 description 7
- 229910052717 sulfur Inorganic materials 0.000 description 5
- SSVJBYATJWWGDE-UHFFFAOYSA-N n-(4-methylphenyl)-3-(5-methylthiophen-2-yl)sulfanyl-1h-1,2,4-triazol-5-amine Chemical compound S1C(C)=CC=C1SC1=NNC(NC=2C=CC(C)=CC=2)=N1 SSVJBYATJWWGDE-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- YKODAWJGNWGCCV-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(2-propan-2-ylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC(C)C1=CC=CC=C1NC1=NC(SC2=C(C=CS2)Cl)=NN1 YKODAWJGNWGCCV-UHFFFAOYSA-N 0.000 description 3
- DHFXQZHZFCRGHS-UHFFFAOYSA-N 3-(3-methylthiophen-2-yl)sulfanyl-n-(2-propan-2-ylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC(C)C1=CC=CC=C1NC1=NC(SC2=C(C=CS2)C)=NN1 DHFXQZHZFCRGHS-UHFFFAOYSA-N 0.000 description 3
- JPZYMONDMULCCK-UHFFFAOYSA-N 3-(5-bromothiophen-2-yl)sulfanyl-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound S1C(Br)=CC=C1SC1=NNC(NC=2C=CC=CC=2)=N1 JPZYMONDMULCCK-UHFFFAOYSA-N 0.000 description 3
- SXXLJBWSUTZQIT-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 SXXLJBWSUTZQIT-UHFFFAOYSA-N 0.000 description 3
- OIATTZYGFPYFAQ-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(2-propan-2-ylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC(C)C1=CC=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 OIATTZYGFPYFAQ-UHFFFAOYSA-N 0.000 description 3
- PXZUQHKCRDCAAE-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(4-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(OC)=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 PXZUQHKCRDCAAE-UHFFFAOYSA-N 0.000 description 3
- PGDTXMNNIGGIQT-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound S1C(Cl)=CC=C1SC1=NNC(NC=2C=CC=CC=2)=N1 PGDTXMNNIGGIQT-UHFFFAOYSA-N 0.000 description 3
- SNUJIKUEACLIOB-UHFFFAOYSA-N 3-(5-methylthiophen-2-yl)sulfanyl-n-(2-propan-2-ylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC(C)C1=CC=CC=C1NC1=NC(SC=2SC(C)=CC=2)=NN1 SNUJIKUEACLIOB-UHFFFAOYSA-N 0.000 description 3
- SWNFXXFBTTZKJP-UHFFFAOYSA-N 3-(5-methylthiophen-2-yl)sulfanyl-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound S1C(C)=CC=C1SC1=NNC(NC=2C=CC=CC=2)=N1 SWNFXXFBTTZKJP-UHFFFAOYSA-N 0.000 description 3
- KFLGMQPKPRSNTG-UHFFFAOYSA-N 3-(furan-2-ylsulfanyl)-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC=3OC=CC=3)N=2)=C1 KFLGMQPKPRSNTG-UHFFFAOYSA-N 0.000 description 3
- FAMZRVODLPRKNL-UHFFFAOYSA-N 3-(furan-2-ylsulfanyl)-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC=2OC=CC=2)=NN1 FAMZRVODLPRKNL-UHFFFAOYSA-N 0.000 description 3
- HYKJHMOWGREVRW-UHFFFAOYSA-N 3-(furan-2-ylsulfanyl)-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=CC=1NC(NN=1)=NC=1SC1=CC=CO1 HYKJHMOWGREVRW-UHFFFAOYSA-N 0.000 description 3
- RDQVJTIXBDRSQR-UHFFFAOYSA-N 3-(furan-3-ylsulfanyl)-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC3=COC=C3)N=2)=C1 RDQVJTIXBDRSQR-UHFFFAOYSA-N 0.000 description 3
- NQKGTBWWTLSAHY-UHFFFAOYSA-N 3-(furan-3-ylsulfanyl)-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC2=COC=C2)=NN1 NQKGTBWWTLSAHY-UHFFFAOYSA-N 0.000 description 3
- XUVZBKHPSIVLBK-UHFFFAOYSA-N 3-(furan-3-ylsulfanyl)-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=CC=1NC(NN=1)=NC=1SC=1C=COC=1 XUVZBKHPSIVLBK-UHFFFAOYSA-N 0.000 description 3
- HSTMOEDERLQUGN-UHFFFAOYSA-N 3-benzylsulfanyl-n-(2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC=C1NC1=NNC(SCC=2C=CC=CC=2)=N1 HSTMOEDERLQUGN-UHFFFAOYSA-N 0.000 description 3
- JVESHYAZMYQQGG-UHFFFAOYSA-N 3-benzylsulfanyl-n-(4-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(OC)=CC=C1NC1=NNC(SCC=2C=CC=CC=2)=N1 JVESHYAZMYQQGG-UHFFFAOYSA-N 0.000 description 3
- VCSAYSMYYHLQSP-UHFFFAOYSA-N CC(C)c1ccccc1Nc1n[nH]c(Sc2ccco2)n1 Chemical compound CC(C)c1ccccc1Nc1n[nH]c(Sc2ccco2)n1 VCSAYSMYYHLQSP-UHFFFAOYSA-N 0.000 description 3
- CUQBEBOKLIGHEG-UHFFFAOYSA-N CC(C)c1ccccc1Nc1n[nH]c(Sc2ccoc2)n1 Chemical compound CC(C)c1ccccc1Nc1n[nH]c(Sc2ccoc2)n1 CUQBEBOKLIGHEG-UHFFFAOYSA-N 0.000 description 3
- DOYJEQSIVADNPC-UHFFFAOYSA-N CC(C)c1ccccc1Nc1n[nH]c(Sc2ccsc2)n1 Chemical compound CC(C)c1ccccc1Nc1n[nH]c(Sc2ccsc2)n1 DOYJEQSIVADNPC-UHFFFAOYSA-N 0.000 description 3
- HFZFNVMFRCEUKL-UHFFFAOYSA-N COc1ccccc1Nc1n[nH]c(Sc2sccc2Cl)n1 Chemical compound COc1ccccc1Nc1n[nH]c(Sc2sccc2Cl)n1 HFZFNVMFRCEUKL-UHFFFAOYSA-N 0.000 description 3
- DEASZYJQDZAWHG-UHFFFAOYSA-N Cc1ccccc1Nc1n[nH]c(Sc2ccco2)n1 Chemical compound Cc1ccccc1Nc1n[nH]c(Sc2ccco2)n1 DEASZYJQDZAWHG-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 150000001350 alkyl halides Chemical class 0.000 description 3
- COUGHWORWINHFG-UHFFFAOYSA-N ethyl 5-[[5-(2-propan-2-ylanilino)-1h-1,2,4-triazol-3-yl]sulfanylmethyl]furan-2-carboxylate Chemical compound O1C(C(=O)OCC)=CC=C1CSC(N1)=NN=C1NC1=CC=CC=C1C(C)C COUGHWORWINHFG-UHFFFAOYSA-N 0.000 description 3
- UZPAVLYUTWNUSX-UHFFFAOYSA-N methyl 4-[(3-benzylsulfanyl-1h-1,2,4-triazol-5-yl)amino]benzoate Chemical compound C1=CC(C(=O)OC)=CC=C1NC1=NNC(SCC=2C=CC=CC=2)=N1 UZPAVLYUTWNUSX-UHFFFAOYSA-N 0.000 description 3
- ZFZNSIGGHKANSR-UHFFFAOYSA-N n-(2-methoxyphenyl)-3-(3-methylthiophen-2-yl)sulfanyl-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NC(SC2=C(C=CS2)C)=NN1 ZFZNSIGGHKANSR-UHFFFAOYSA-N 0.000 description 3
- UIDVAHJHCAALOW-UHFFFAOYSA-N n-(2-methoxyphenyl)-3-(5-methylthiophen-2-yl)sulfanyl-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NC(SC=2SC(C)=CC=2)=NN1 UIDVAHJHCAALOW-UHFFFAOYSA-N 0.000 description 3
- XYVXLHYAPXUTFD-UHFFFAOYSA-N n-(3-methylphenyl)-3-thiophen-3-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC3=CSC=C3)N=2)=C1 XYVXLHYAPXUTFD-UHFFFAOYSA-N 0.000 description 3
- HOQOTPFYKDHPPO-UHFFFAOYSA-N n-(3-thiophen-2-ylsulfanyl-1h-1,2,4-triazol-5-yl)pyridin-3-amine Chemical compound C=1C=CN=CC=1NC(N=1)=NNC=1SC1=CC=CS1 HOQOTPFYKDHPPO-UHFFFAOYSA-N 0.000 description 3
- KOLIQRWULWBTRO-UHFFFAOYSA-N n-(4-chlorophenyl)-3-thiophen-2-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(Cl)=CC=C1NC1=NC(SC=2SC=CC=2)=NN1 KOLIQRWULWBTRO-UHFFFAOYSA-N 0.000 description 3
- PJHSVELYXUUXPI-UHFFFAOYSA-N n-(4-methylphenyl)-3-thiophen-2-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC=2SC=CC=2)=NN1 PJHSVELYXUUXPI-UHFFFAOYSA-N 0.000 description 3
- OITROJOEWSTWIW-UHFFFAOYSA-N n-(4-methylphenyl)-3-thiophen-3-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC2=CSC=C2)=NN1 OITROJOEWSTWIW-UHFFFAOYSA-N 0.000 description 3
- VBSSVYJFFVJXDJ-UHFFFAOYSA-N n-phenyl-3-thiophen-2-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=CC=1NC(NN=1)=NC=1SC1=CC=CS1 VBSSVYJFFVJXDJ-UHFFFAOYSA-N 0.000 description 3
- CSOPOFJNZYJZJH-UHFFFAOYSA-N n-phenyl-3-thiophen-3-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=CC=1NC(NN=1)=NC=1SC=1C=CSC=1 CSOPOFJNZYJZJH-UHFFFAOYSA-N 0.000 description 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 2
- PWXLEAVSSVXZGL-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC=C1NC1=NC(SC2=C(C=CS2)Cl)=NN1 PWXLEAVSSVXZGL-UHFFFAOYSA-N 0.000 description 2
- CQUIZEMQWMKVMY-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC3=C(C=CS3)Cl)N=2)=C1 CQUIZEMQWMKVMY-UHFFFAOYSA-N 0.000 description 2
- CWCKONMZORSQQK-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(4-fluorophenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(F)=CC=C1NC1=NC(SC2=C(C=CS2)Cl)=NN1 CWCKONMZORSQQK-UHFFFAOYSA-N 0.000 description 2
- WRHMZDXBDXXIGK-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(4-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(OC)=CC=C1NC1=NC(SC2=C(C=CS2)Cl)=NN1 WRHMZDXBDXXIGK-UHFFFAOYSA-N 0.000 description 2
- DABRIDCJWJCDLJ-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC2=C(C=CS2)Cl)=NN1 DABRIDCJWJCDLJ-UHFFFAOYSA-N 0.000 description 2
- AMVHNDJLVTVGAU-UHFFFAOYSA-N 3-(3-chlorothiophen-2-yl)sulfanyl-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound C1=CSC(SC=2N=C(NC=3C=CC=CC=3)NN=2)=C1Cl AMVHNDJLVTVGAU-UHFFFAOYSA-N 0.000 description 2
- DHHDNUXVQYYLPA-UHFFFAOYSA-N 3-(3-methylthiophen-2-yl)sulfanyl-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound C1=CSC(SC=2N=C(NC=3C=CC=CC=3)NN=2)=C1C DHHDNUXVQYYLPA-UHFFFAOYSA-N 0.000 description 2
- HDDJDZDOKRLEPS-UHFFFAOYSA-N 3-(5-bromothiophen-2-yl)sulfanyl-n-(2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC=C1NC1=NC(SC=2SC(Br)=CC=2)=NN1 HDDJDZDOKRLEPS-UHFFFAOYSA-N 0.000 description 2
- GKLBIFMCIQKIDU-UHFFFAOYSA-N 3-(5-bromothiophen-2-yl)sulfanyl-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC=3SC(Br)=CC=3)N=2)=C1 GKLBIFMCIQKIDU-UHFFFAOYSA-N 0.000 description 2
- XOLYXWLLWMSDIJ-UHFFFAOYSA-N 3-(5-bromothiophen-2-yl)sulfanyl-n-(4-fluorophenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(F)=CC=C1NC1=NC(SC=2SC(Br)=CC=2)=NN1 XOLYXWLLWMSDIJ-UHFFFAOYSA-N 0.000 description 2
- CWAAIZHOPULLPV-UHFFFAOYSA-N 3-(5-bromothiophen-2-yl)sulfanyl-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC=2SC(Br)=CC=2)=NN1 CWAAIZHOPULLPV-UHFFFAOYSA-N 0.000 description 2
- IYHOHLKHYHPVSM-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 IYHOHLKHYHPVSM-UHFFFAOYSA-N 0.000 description 2
- UEKXWPIQOLHYDC-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2NN=C(SC=3SC(Cl)=CC=3)N=2)=C1 UEKXWPIQOLHYDC-UHFFFAOYSA-N 0.000 description 2
- DDPXOOBFZFRAKM-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(4-fluorophenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(F)=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 DDPXOOBFZFRAKM-UHFFFAOYSA-N 0.000 description 2
- VDWMFPWXQFRLSC-UHFFFAOYSA-N 3-(5-chlorothiophen-2-yl)sulfanyl-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NC(SC=2SC(Cl)=CC=2)=NN1 VDWMFPWXQFRLSC-UHFFFAOYSA-N 0.000 description 2
- ZGYUDXYEKJBWGQ-UHFFFAOYSA-N 3-(furan-2-ylsulfanyl)-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NC(SC=2OC=CC=2)=NN1 ZGYUDXYEKJBWGQ-UHFFFAOYSA-N 0.000 description 2
- SMQLCSMMAKTBSJ-UHFFFAOYSA-N 3-(furan-3-ylsulfanyl)-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NC(SC2=COC=C2)=NN1 SMQLCSMMAKTBSJ-UHFFFAOYSA-N 0.000 description 2
- NAFJUZKFEUUDKV-UHFFFAOYSA-N 3-[(2-fluorophenyl)methylsulfanyl]-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NNC(SCC=2C(=CC=CC=2)F)=N1 NAFJUZKFEUUDKV-UHFFFAOYSA-N 0.000 description 2
- NXBLUWQGGLQYQM-UHFFFAOYSA-N 3-[(2-fluorophenyl)methylsulfanyl]-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2N=C(SCC=3C(=CC=CC=3)F)NN=2)=C1 NXBLUWQGGLQYQM-UHFFFAOYSA-N 0.000 description 2
- GDZHHXOYXPKDLO-UHFFFAOYSA-N 3-[(2-fluorophenyl)methylsulfanyl]-n-(4-methoxy-2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC(OC)=CC=C1NC1=NNC(SCC=2C(=CC=CC=2)F)=N1 GDZHHXOYXPKDLO-UHFFFAOYSA-N 0.000 description 2
- UBZUXVQIHHRQHG-UHFFFAOYSA-N 3-[(2-fluorophenyl)methylsulfanyl]-n-(4-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(OC)=CC=C1NC1=NNC(SCC=2C(=CC=CC=2)F)=N1 UBZUXVQIHHRQHG-UHFFFAOYSA-N 0.000 description 2
- YYIJNRPVYDYLRE-UHFFFAOYSA-N 3-[(2-fluorophenyl)methylsulfanyl]-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NNC(SCC=2C(=CC=CC=2)F)=N1 YYIJNRPVYDYLRE-UHFFFAOYSA-N 0.000 description 2
- PPUFZAUHFAXGBM-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(2,4-dimethoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC(OC)=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 PPUFZAUHFAXGBM-UHFFFAOYSA-N 0.000 description 2
- CNWQUDKZKSKAST-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(2,6-dimethylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(C)=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 CNWQUDKZKSKAST-UHFFFAOYSA-N 0.000 description 2
- FFIDUOXKZSOIBZ-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(2-ethylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CCC1=CC=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 FFIDUOXKZSOIBZ-UHFFFAOYSA-N 0.000 description 2
- LCGRNWJSKOHUBU-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 LCGRNWJSKOHUBU-UHFFFAOYSA-N 0.000 description 2
- AQBIMSLMBXMPSV-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 AQBIMSLMBXMPSV-UHFFFAOYSA-N 0.000 description 2
- ZEHXHMKMTHWBQY-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(3,4-dimethoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=C(OC)C(OC)=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 ZEHXHMKMTHWBQY-UHFFFAOYSA-N 0.000 description 2
- OIYTXJVMQLCGKD-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2N=C(SCC=3C=C(F)C(F)=CC=3)NN=2)=C1 OIYTXJVMQLCGKD-UHFFFAOYSA-N 0.000 description 2
- CQFAERVRCDLGBQ-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(4-methoxy-2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC(OC)=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 CQFAERVRCDLGBQ-UHFFFAOYSA-N 0.000 description 2
- JCCLYBLQSDKYDK-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-(4-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NNC(SCC=2C=C(F)C(F)=CC=2)=N1 JCCLYBLQSDKYDK-UHFFFAOYSA-N 0.000 description 2
- KTWYUXALXXVYQE-UHFFFAOYSA-N 3-[(3,4-difluorophenyl)methylsulfanyl]-n-phenyl-1h-1,2,4-triazol-5-amine Chemical compound C1=C(F)C(F)=CC=C1CSC1=NC(NC=2C=CC=CC=2)=NN1 KTWYUXALXXVYQE-UHFFFAOYSA-N 0.000 description 2
- MKZCDFBGFBYCCQ-UHFFFAOYSA-N 3-[(4-fluorophenyl)methylsulfanyl]-n-(2-methoxyphenyl)-1h-1,2,4-triazol-5-amine Chemical compound COC1=CC=CC=C1NC1=NNC(SCC=2C=CC(F)=CC=2)=N1 MKZCDFBGFBYCCQ-UHFFFAOYSA-N 0.000 description 2
- MWNYEANTJBPRNF-UHFFFAOYSA-N 3-[(4-fluorophenyl)methylsulfanyl]-n-(3-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC=CC(NC=2N=C(SCC=3C=CC(F)=CC=3)NN=2)=C1 MWNYEANTJBPRNF-UHFFFAOYSA-N 0.000 description 2
- CVZWCPNYLAZZKB-UHFFFAOYSA-N 3-[(4-fluorophenyl)methylsulfanyl]-n-(4-methoxy-2-methylphenyl)-1h-1,2,4-triazol-5-amine Chemical compound CC1=CC(OC)=CC=C1NC1=NNC(SCC=2C=CC(F)=CC=2)=N1 CVZWCPNYLAZZKB-UHFFFAOYSA-N 0.000 description 2
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- GSJJLAZCTRDKSS-UHFFFAOYSA-N n-(4-methylphenyl)-3-[(2-methylphenyl)methylsulfanyl]-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C)=CC=C1NC1=NNC(SCC=2C(=CC=CC=2)C)=N1 GSJJLAZCTRDKSS-UHFFFAOYSA-N 0.000 description 1
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- LJYQBCYDGPEXAJ-UHFFFAOYSA-N n-[3-(pyridin-2-ylmethylsulfanyl)-1h-1,2,4-triazol-5-yl]pyridin-3-amine Chemical compound C=1C=CC=NC=1CSC(NN=1)=NC=1NC1=CC=CN=C1 LJYQBCYDGPEXAJ-UHFFFAOYSA-N 0.000 description 1
- SQQSUMIEMWCUGN-UHFFFAOYSA-N n-[3-(pyridin-4-ylmethylsulfanyl)-1h-1,2,4-triazol-5-yl]pyridin-3-amine Chemical compound C=1C=NC=CC=1CSC(NN=1)=NC=1NC1=CC=CN=C1 SQQSUMIEMWCUGN-UHFFFAOYSA-N 0.000 description 1
- QTVZODFEDWSCGZ-UHFFFAOYSA-N n-[3-[(2-methyl-1,3-thiazol-4-yl)methylsulfanyl]-1h-1,2,4-triazol-5-yl]pyridin-3-amine Chemical compound S1C(C)=NC(CSC=2NN=C(NC=3C=NC=CC=3)N=2)=C1 QTVZODFEDWSCGZ-UHFFFAOYSA-N 0.000 description 1
- HJPZWWYALIMYCP-UHFFFAOYSA-N n-[3-[(2-methylphenyl)methylsulfanyl]-1h-1,2,4-triazol-5-yl]pyridin-3-amine Chemical compound CC1=CC=CC=C1CSC1=NC(NC=2C=NC=CC=2)=NN1 HJPZWWYALIMYCP-UHFFFAOYSA-N 0.000 description 1
- AACDUZATGDPUNH-UHFFFAOYSA-N n-[3-[(5-methyl-1,2-oxazol-3-yl)methylsulfanyl]-1h-1,2,4-triazol-5-yl]pyridin-3-amine Chemical compound O1C(C)=CC(CSC=2NN=C(NC=3C=NC=CC=3)N=2)=N1 AACDUZATGDPUNH-UHFFFAOYSA-N 0.000 description 1
- RMPZMLWBDBTEMQ-UHFFFAOYSA-N n-[4-[(5-anilino-1h-1,2,4-triazol-3-yl)sulfanylmethyl]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1CSC1=NC(NC=2C=CC=CC=2)=NN1 RMPZMLWBDBTEMQ-UHFFFAOYSA-N 0.000 description 1
- BRXROFPDDHOZMB-UHFFFAOYSA-N n-phenyl-3-(1-phenylethylsulfanyl)-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=CC=1C(C)SC(NN=1)=NC=1NC1=CC=CC=C1 BRXROFPDDHOZMB-UHFFFAOYSA-N 0.000 description 1
- KLPYJLQTNSIDDN-UHFFFAOYSA-N n-phenyl-3-(2-phenylethylsulfanyl)-1h-1,2,4-triazol-5-amine Chemical compound N=1C(NC=2C=CC=CC=2)=NNC=1SCCC1=CC=CC=C1 KLPYJLQTNSIDDN-UHFFFAOYSA-N 0.000 description 1
- JTWLGXZNCKQFMS-UHFFFAOYSA-N n-phenyl-3-(pyridin-2-ylmethylsulfanyl)-1h-1,2,4-triazol-5-amine Chemical compound C=1C=CC=NC=1CSC(NN=1)=NC=1NC1=CC=CC=C1 JTWLGXZNCKQFMS-UHFFFAOYSA-N 0.000 description 1
- OOUAOHZMQRNZLU-UHFFFAOYSA-N n-phenyl-3-(pyridin-4-ylmethylsulfanyl)-1h-1,2,4-triazol-5-amine Chemical compound C=1C=NC=CC=1CSC(NN=1)=NC=1NC1=CC=CC=C1 OOUAOHZMQRNZLU-UHFFFAOYSA-N 0.000 description 1
- GBFGPNJGRVHHGX-UHFFFAOYSA-N n-phenyl-3-[[4-(trifluoromethyl)phenyl]methylsulfanyl]-1h-1,2,4-triazol-5-amine Chemical compound C1=CC(C(F)(F)F)=CC=C1CSC1=NC(NC=2C=CC=CC=2)=NN1 GBFGPNJGRVHHGX-UHFFFAOYSA-N 0.000 description 1
- BYHCYCFRDSXURW-UHFFFAOYSA-N n-phenyl-3-quinolin-8-ylsulfanyl-1h-1,2,4-triazol-5-amine Chemical compound N=1NC(SC=2C3=NC=CC=C3C=CC=2)=NC=1NC1=CC=CC=C1 BYHCYCFRDSXURW-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 235000020824 obesity Nutrition 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- NHDZOMNMBJBILW-UHFFFAOYSA-N s-(5-anilino-1h-1,2,4-triazol-3-yl) pentanethioate Chemical compound N1C(SC(=O)CCCC)=NC(NC=2C=CC=CC=2)=N1 NHDZOMNMBJBILW-UHFFFAOYSA-N 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
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| EP1381360A4 (en) * | 2001-03-29 | 2009-12-02 | Smithkline Beecham Corp | COMPOUNDS AND METHODS FOR INHIBITING METAP2 IN MAMMALS |
| AU2003223357A1 (en) * | 2002-03-27 | 2003-10-13 | Smithkline Beecham Corporation | Compounds and methods |
| IL166510A0 (en) * | 2002-08-09 | 2006-01-15 | Nps Pharma Inc | 1,2,4"oxadiazole as modulators of metabotropic glutamate receptor-5 |
| FR2862060A1 (fr) * | 2003-11-06 | 2005-05-13 | Galderma Res & Dev | Procede de synthese en phase solide de composes de types sulfures de diaryle. |
| EP2026797A2 (en) * | 2006-05-25 | 2009-02-25 | Synta Pharmaceuticals Corporation | Method for treating non-hodgkin's lymphoma |
| EP2170402B1 (en) | 2007-06-26 | 2015-03-25 | Children's Medical Center Corporation | Metap-2 inhibitor polymersomes for therapeutic administration |
| WO2013055385A2 (en) | 2011-10-03 | 2013-04-18 | Zafgen Corporation | Methods of treating age related disorders |
| CA2777108A1 (en) | 2009-10-09 | 2011-04-14 | Zafgen Corporation | Sulphone compounds and methods of making and using same |
| US8815309B2 (en) | 2010-01-08 | 2014-08-26 | Zafgen, Inc. | Methods of treating a subject with benign prostate hyperplasia |
| WO2011088055A2 (en) | 2010-01-12 | 2011-07-21 | Zafgen Corporation | Methods and compositions for treating cardiovascular disorders |
| WO2011127304A2 (en) | 2010-04-07 | 2011-10-13 | Zafgen Corporation | Methods of treating an overweight subject |
| US9205086B2 (en) | 2010-04-19 | 2015-12-08 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor |
| CN103249735B (zh) * | 2010-07-22 | 2016-04-06 | 扎夫根股份有限公司 | 三环化合物及其制备和使用方法 |
| WO2012064928A1 (en) | 2010-11-10 | 2012-05-18 | Zafgen Corporation | Methods and compositions for treating thyroid hormone related disorders |
| WO2012074968A1 (en) | 2010-11-29 | 2012-06-07 | Zafgen Corporation | Methods of reducing risk of hepatobiliary dysfunction during rapid weight loss with metap-2 inhibitors |
| US9189078B2 (en) | 2010-12-20 | 2015-11-17 | Apple Inc. | Enhancing keycap legend visibility with optical components |
| MX344238B (es) | 2011-01-26 | 2016-12-07 | Zafgen Inc | Compuestos de tetrazol y métodos para preparar y usar los mismos. |
| CN103764641B (zh) | 2011-05-06 | 2016-10-26 | 扎夫根股份有限公司 | 部分饱和的三环化合物及其制备和使用方法 |
| EP2705036B1 (en) | 2011-05-06 | 2015-08-12 | Zafgen Inc. | Tricyclic sulfonamide compounds and methods of making and using same |
| BR112013028666A2 (pt) | 2011-05-06 | 2017-08-08 | Zafgen Inc | compostos de pirazolo sulfonamida tricícilos e métodos para fazer e usar o mesmo |
| AU2012332424A1 (en) | 2011-11-02 | 2014-06-05 | Synta Pharmaceuticals Corp. | Combination therapy of Hsp90 inhibitors with platinum-containing agents |
| EP2773345A1 (en) | 2011-11-02 | 2014-09-10 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors |
| WO2013074594A1 (en) | 2011-11-14 | 2013-05-23 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with braf inhibitors |
| MX2014008706A (es) | 2012-01-18 | 2015-03-05 | Zafgen Inc | Compuestos tricíclicos de sulfonamida y métodos para elaborarlos y usarlos. |
| JP2015509102A (ja) | 2012-01-18 | 2015-03-26 | ザフゲン，インコーポレイテッド | 三環式スルホン化合物並びにその作製および使用方法 |
| MX2014013599A (es) | 2012-05-08 | 2015-05-11 | Zafgen Inc | Tratamiento de la obesidad hipotalamica con inhibidores de metap2. |
| BR112014027981A2 (pt) | 2012-05-09 | 2017-06-27 | Zafgen Inc | compostos do tipo fumagilol e métodos de produção e utilização dos mesmos |
| NZ707773A (en) | 2012-11-05 | 2019-05-31 | Zafgen Inc | Methods of treating liver diseases |
| AU2013337282A1 (en) | 2012-11-05 | 2015-05-21 | Zafgen, Inc. | Tricyclic compounds and methods of making and using same |
| MX2015005733A (es) | 2012-11-05 | 2016-02-10 | Zafgen Inc | Compuestos triciclicos para usarse en el tratamiento y/o control de obesidad. |
| CN105228610A (zh) | 2013-03-14 | 2016-01-06 | 扎夫根股份有限公司 | 治疗肾疾病和其它病症的方法 |
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| US10323016B2 (en) * | 2014-06-12 | 2019-06-18 | Universite De Lille 2 Droit Et Sante | Imidazol- or 1,2,4-triazol-derivatives and their use |
| CN106432255A (zh) | 2015-08-11 | 2017-02-22 | 扎夫根公司 | 烟曲霉素醇螺环化合物和制备和使用其的方法 |
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| MX2020011501A (es) * | 2018-05-04 | 2020-12-07 | Inflazome Ltd | Compuestos novedosos. |
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| US4760448A (en) * | 1987-05-04 | 1988-07-26 | Sencore, Inc. | Method of measuring amplitude variations of a video carrier and apparatus therefor |
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| GB9207396D0 (en) | 1992-04-03 | 1992-05-13 | Merck Sharp & Dohme | Therapeutic agents |
| DE4424787A1 (de) | 1994-07-14 | 1996-01-18 | Bayer Ag | Substituierte Aryliminoheterocyclen |
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| US5798374A (en) * | 1995-06-07 | 1998-08-25 | Sugen Inc. | Methods of inhibiting phosphatase activity and treatment of disorders associated therewith |
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| DE19922443A1 (de) * | 1999-05-07 | 2000-11-09 | Basf Ag | Verwendung von Dopamin-D3-Rezeptorliganden zur Herstellung von Arzneimittel für die Behandlung von Nierenfunktionsstörungen |
| DE19921567A1 (de) * | 1999-05-11 | 2000-11-16 | Basf Ag | Verwendung von Phthalazine-Derivaten |
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| HN2001000008A (es) * | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | Compuesto de amida y composiciones farmaceuticas para inhibir proteinquinasas, y su modo de empleo |
| US20030220371A1 (en) * | 2000-04-12 | 2003-11-27 | Kallander Lara S. | Compounds and methods |
| AU2001278951A1 (en) | 2000-07-19 | 2002-01-30 | Smith Kline Beecham Corporation | Compounds and methods |
| US20060247280A1 (en) | 2001-03-29 | 2006-11-02 | Marino Joseph P Jr | Compounds and methods |
| JP2004525942A (ja) | 2001-03-29 | 2004-08-26 | スミスクライン・ビーチャム・コーポレイション | 化合物および方法 |
| AU2002306907A1 (en) | 2001-04-03 | 2002-10-21 | Smithkline Beecham Corporation | Method for inhibiting metap2 |
| WO2003031434A1 (en) | 2001-10-12 | 2003-04-17 | Smith Kline Beecham Corporation | Compounds and methods |
| WO2003051906A2 (en) | 2001-12-14 | 2003-06-26 | Smithkline Beecham Corporation | Compounds and methods |
| JP2003281388A (ja) | 2002-03-25 | 2003-10-03 | Hitachi Ltd | 自動取引装置 |
| AU2003223357A1 (en) | 2002-03-27 | 2003-10-13 | Smithkline Beecham Corporation | Compounds and methods |
| US20040116490A1 (en) | 2002-03-28 | 2004-06-17 | Marino Jr. Joseph P. | Compounds and methods |
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- 2000-09-29 WO PCT/US2000/026951 patent/WO2001024796A1/en not_active Ceased
- 2000-09-29 JP JP2001527795A patent/JP2003510359A/ja active Pending
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2005
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