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Cc1ccc(Nc2cccnc2)cc1

C#Cc1ccc(Nc2cnccc2C(=O)NOCC(O)CO)c(Cl)c1
Reaction #67835
desired product
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
المردود 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2ccc(Br)nc2)c(C(=O)OC(C)(C)C)c1
Reaction #70281
expected product
المردود 40.2%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(C2CC2)ccc1Nc1ccc(Br)nc1
Reaction #70283
Methyl 2-(6-bromopyridin-3-ylamino)-5-cyclopropylbenzoate
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
المردود 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
المردود 20.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(C3CC3)c(C)c2)c(C(=O)O)c1
Reaction #70331
expected product
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(Nc2ccc(C3CC3)cc2C(=O)O)cnc1-c1ccccc1
Reaction #70332
expected product
المردود 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
المردود 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
Cc1ccc(Nc2cnc(-c3ccccc3)c(Cl)c2)c(C(=O)OC(C)(C)C)c1
Reaction #70337
tert-Butyl 2-(5-chloro-6-phenylpyridin-3-ylamino)-5-methylbenzoate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(Nc2cnc(-c3ccccc3)c(Cl)c2)c(C(=O)O)c1
Reaction #70338
2-(5-Chloro-6-phenylpyridin-3-ylamino)-5-methylbenzoic 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
المردود 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(Nc2ccc(N3CCOCC3)nc2)c(C(=O)O)c1
Reaction #70344
expected product
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
المردود 62.0%DOI: 10.6084/m9.figshare.5104873.v1
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