#1122

CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C#N
Reaction #129
المردود 50.0%750 AstraZeneca ELN dataset
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #131
المردود 7.3%750 AstraZeneca ELN dataset
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #132
المردود 54.9%750 AstraZeneca ELN dataset
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #133
المردود 43.8%750 AstraZeneca ELN dataset
Cc1nn(C)cc1Nc1cc(Nc2cccc3c2C(=O)N(C)CC3)c(C#N)cn1
Reaction #134
المردود 15.6%750 AstraZeneca ELN dataset
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #146
المردود 14.3%750 AstraZeneca ELN dataset
CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #157
المردود 53.3%750 AstraZeneca ELN dataset
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C(F)(F)F
Reaction #170
المردود 11.2%750 AstraZeneca ELN dataset
CNC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1C(F)(F)F
Reaction #172
المردود 33.7%750 AstraZeneca ELN dataset
CONC(=O)c1ccccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #90782
desired product
المردود 18.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CNC(=O)c1cc(F)ccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #198975
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(=O)Nc1cn(C)nc1C
Reaction #407335
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
Cc1nn(C)cc1Nc1c([N+](=O)[O-])cnc2ccc(Br)cc12
Reaction #532721
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
Cc1nn(C)cc1Nc1cnc2c(n1)c(C(=O)NC(C)(C)C)cn2COCC[Si](C)(C)C
Reaction #610186
N-tert-butyl-2-(1,3-dimethyl-1H-pyrazol-4-ylamino)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide
المردود 55.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_05
Cc1nn(C)cc1Nc1ncc(Cl)c(CCc2ccccc2C2(C(N)=O)CC2)n1
Reaction #679587
title compound 26
المردود 25.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_01
CCOC(=O)c1cnc2ccc(-c3ccc(OC)c(OC)c3)nc2c1Nc1cn(C)nc1C
Reaction #775469
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COc1cc(OCc2ccccc2)ccc1CC(=O)Nc1cn(C)nc1C
Reaction #1096939
N-(1,3-dimethylpyrazol-4-yl)-2-(4-benzyloxy-2-methoxyphenyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2011_07
CNC(=O)c1cc(F)ccc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #1133115
2-(5-chloro-2-(1,3-dimethyl-1H-pyrazol-4-ylamino)pyridin-4-ylamino)-5-fluoro-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CNC(=O)c1ccc(F)cc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #1133116
2-(5-chloro-2-(1,3-dimethyl-1H-pyrazol-4-ylamino)pyridin-4-ylamino)-4-fluoro-N-methylbenzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
CNC(=O)c1ccc(F)cc1Nc1cc(Nc2cn(C)nc2C)ncc1Cl
Reaction #1233892
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
الصفحة 1التالي