5-methyl-1,3-thiazole-2-carboxylic acid

Cc1cnc(C(=O)N[C@@H](C)[C@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)c2ccc(C)c(C)c2)s1
Reaction #41467
N-[(1R,2S)-1-(3,4-dimethylphenyl)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-propan-2-yl]-5-methyl-1,3-thiazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2ncc(C)s2)c1
Reaction #41471
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2yl]-5-methyl-1,3-thiazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1cnc(C(=O)Nc2cccc(N(C)c3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #264103
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #395560
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #811551
5-Methyl-thiazole-2-carboxylic acid{3-(3-styryl-1H-indazol-6-yloxy)-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
Cc1cnc(C(=O)Nc2cccc(N(C)c3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #811566
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_11
Cc1cnc(C(=O)N[C@H](C)Cn2ccc(-c3ccc(C#N)c(Cl)c3)n2)s1
Reaction #959763
title compound
Rendimiento 54.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_03
COc1cccc(C(Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)C(C)NC(=O)c2ncc(C)s2)c1
Reaction #1043577
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
Cc1cnc(C(=O)N[C@@H](C)[C@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)c2ccc(C)c(C)c2)s1
Reaction #1186132
N-[(1R,2S)-1-(3,4-dimethylphenyl)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-propan-2-yl]-5-methyl-1,3-thiazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COc1cccc([C@@H](Oc2ccc3c(cnn3-c3ccc(F)cc3)c2)[C@H](C)NC(=O)c2ncc(C)s2)c1
Reaction #1186138
N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]-5-methyl-1,3-thiazole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
Cc1cnc(C(=O)NNC(=O)OC(C)(C)C)s1
Reaction #1622491
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #1903975
5-Methyl-thiazole-2-carboxylic acid {3-(3-styryl-1H-indazol-6-yloxy)-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_04
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #1948243
5-Methyl-thiazole-2-carboxylic Acid {3-(3-Styryl-1H-indazol-6-yloxy)-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
Cc1cnc(C(=O)Nc2cccc(N(C)c3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #1948259
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #1949286
5-Methyl-thiazole-2-carboxylic Acid {3-(3-Styryl-1H-indazol-6-yloxy)-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
Cc1cnc(C(=O)Nc2cccc(N(C)c3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #1949300
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2003_03
Cc1cnc(C(=O)NNC(=O)OC(C)(C)C)s1
Reaction #1976227
desired product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_08
Cc1cnc(C(=O)Nc2cnc(OCC(F)(F)F)c(-c3ccc(Cl)cc3)c2)s1
Reaction #2045309
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
Cc1cnc(C(=O)Nc2cccc(Oc3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #2268688
5-Methyl-thiazole-2-carboxylic acid {3-(3-styryl-1H-indazol-6-yloxy)-phenyl]-amide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_05
Cc1cnc(C(=O)Nc2cccc(N(C)c3ccc4c(C=Cc5ccccc5)n[nH]c4c3)c2)s1
Reaction #2268700
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_05
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