部分構造検索

8412883

O=C(O)c1cc2c(c(C(=O)O)c1)NCCCC2
Reaction #5029
compound
収率 85.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(N)c([N+](=O)[O-])cc(-c2ccn(C)c(=O)c2)c1F
Reaction #40529
title compound
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NCc1cc(C(=O)O)c(Nc2ccc(I)cc2F)c(F)c1F
Reaction #49053
5-(tert-butoxycarbonylamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc(Cl)nc2)c(C(=O)O)c1
Reaction #70280
2-(6-Chloropyridin-3-ylamino)-5-methylbenzoic acid
収率 46.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1Nc1cnc(Cl)nc1
Reaction #70282
expected product
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)ccc1Nc1cnc(Br)c(C)c1
Reaction #70320
Ethyl 2-(6-bromo-5-methylpyridin-3-ylamino)-5-methylbenzoate
収率 25.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(Br)c(C)c2)c(C(=O)O)c1
Reaction #70323
2-(6-Bromo-5-methylpyridin-3-ylamino)-5-methylbenzoic acid
収率 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2ccc(C3CC3)cc2C(=O)O)cnc1-c1ccccc1
Reaction #70332
expected product
収率 29.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2ccc(C3CC3)cc2C(=O)O)c[n+]([O-])c1-c1ccccc1
Reaction #70333
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(O)c(-c2ccccc2)c1
Reaction #70334
5-Cyclopropyl-2-(6-hydroxy-5-phenylpyridin-3-ylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
COc1ncc(Nc2ccc(C3CC3)cc2C(=O)O)cc1-c1ccccc1
Reaction #70335
expected product
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3)c(F)c2)c(C(=O)O)c1
Reaction #70336
expected product
DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(-c2ccccc2Cl)nc1
Reaction #70339
expected product
収率 81.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1cc(C2CC2)ccc1Nc1cnc(-c2ccccc2C2CC2)nc1
Reaction #70340
5-Cyclopropyl-2-(2-(2-cyclopropylphenyl)pyrimidin-5-ylamino)benzoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cc(C)ccc1Nc1cnc2ccccc2c1
Reaction #70341
Ethyl 5-methyl-2-(quinolin-3-ylamino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc3c(c2)CCCC3)c(C(=O)O)c1
Reaction #70342
desired compound
収率 79.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cc(Cl)cnc2-c2ccccc2)c(C(=O)OC(C)(C)C)c1
Reaction #70343
tert-Butyl 2-(5-chloro-2-phenylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3C3CC3)c(C)c2)c(C(=O)OC(C)(C)C)c1
Reaction #70345
tert-Butyl 2-(6-(2-cyclopropylphenyl)-5-methylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc(-c3ccncc3Cl)nc2)c(C(=O)O)c1
Reaction #70346
expected product
収率 62.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(F)c(F)c2)c(C(=O)O)c1
Reaction #70347
expected product
収率 15.0%DOI: 10.6084/m9.figshare.5104873.v1
1 ページ次のページ