部分構造検索

157171

CCOC(=O)c1cnn(-c2cc(C(=O)NC)ccc2Cl)c1C1CC1
Reaction #255435
DOI: 10.1039/C8SC04228D
CNC(=O)c1cnn(-c2ccc(Cl)cc2Cl)c1C#N
Reaction #367635
5-cyano-1-(2,4-dichlorophenyl)-N-methyl-1H-pyrazole-4-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(-c2cc(S(=O)(=O)Cl)ccc2Cl)c1C1CC1
Reaction #373123
DOI: 10.1039/C8SC04228D
Cc1c(C(=O)O)cnn1-c1c(Cl)cc(Cl)cc1Cl
Reaction #389349
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnn(-c2cc(S(=O)(=O)N(C)C)ccc2Cl)c1C1CC1
Reaction #406422
DOI: 10.1039/C8SC04228D
CS(=O)(=O)c1ccc(-n2ncc(C(=O)NC(=N)N)c2C2CC2)c(Cl)c1
Reaction #440626
N-{5-cyclopropyl-1-(2-chloro-4-methanesulfonylphenyl)-1H-pyrazole-4-carbonyl}-guanidine
DOI: 10.6084/m9.figshare.5104873.v1
N=C(N)NC(=O)c1cnn(-c2cccc3ncccc23)c1C1CC1
Reaction #440627
N-(5-cyclopropyl-1-quinolin-5-yl-1H-pyrazole-4-carbonyl)-guanidine
DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2ncc(C(=O)O)c2C2CC2)c(Cl)c1
Reaction #440628
5-cyclopropyl-1-(2-chloro-4-methanesulfonylphenyl)-1H-pyrazole-4-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(-c2cc(S(=O)(=O)Cl)ccc2Cl)c1C1CC1
Reaction #575982
ethyl 5-cyclopropyl-1-(2-chloro-5-{chlorosulfonyl}phenyl)-1H-pyrazole-4-carboxylate
収率 95.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(-c2cc(S(=O)(=O)N(C)C)ccc2Cl)c1C1CC1
Reaction #575983
desired product
収率 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnn(-c2cc(C(=O)NC)ccc2Cl)c1C1CC1
Reaction #575984
title compound
収率 77.1%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(SC)nn(-c2c(Cl)cc(Cl)cc2Cl)c1C
Reaction #706490
desired product
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c(CC)c1C(=O)OC
Reaction #706492
desired product
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1c(C(=O)O)cnn1-c1ccc(Cl)cc1Cl
Reaction #772863
DOI: 10.1039/C8SC04228D
Cc1c(C(=O)Nc2ccc(N3CCC(N4CCOCC4)CC3)c(C#N)c2)cnn1-c1ccccc1Cl
Reaction #789177
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(SC)nn(-c2c(Cl)cc(Cl)cc2Cl)c1C
Reaction #812451
desired product
収率 56.4%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c(CC)c1C(=O)OC
Reaction #812453
desired product
収率 43.0%DOI: 10.6084/m9.figshare.5104873.v1
CCc1nn(-c2c(Cl)cc(C(F)(F)F)cc2Cl)c(CC)c1CO
Reaction #812454
title compound
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cnn(-c2ccc(Cl)cc2Cl)c1C(F)(F)F
Reaction #909277
DOI: 10.1039/C8SC04228D
CNC(=O)c1cnn(-c2ccc(Cl)cc2Cl)c1C#N
Reaction #920161
DOI: 10.1039/C8SC04228D
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