2-chloropyridine-3-carbonitrile

Cc1ncccc1C#N
Reaction #7249
desired product
수율 46.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(Cc1c[nH]c2c(Oc3ncccc3C#N)cccc12)NC(=O)OC(C)(C)C
Reaction #8195
{2-[7-(3-cyano-pyridin-2-yloxy)-1H-indol-3-yl]-1,1-dimethyl-ethyl}-carbamic acid tert-butyl ester
수율 96.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
CC(C)(C)OC(=O)N1CCCC[C@H]1CNc1ncccc1C#N
Reaction #46377
title compound
수율 28.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
COc1ccc(CNc2ncccc2C#N)c(OC)c1
Reaction #48380
title compound
수율 72.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1cccnc1SCc1ccccc1
Reaction #48526
2-(phenyl methyl thio)-3-cyanopyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
CCOC(=O)c1sc2ncccc2c1N
Reaction #58696
title compound
수율 93.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cl.N#Cc1cccnc1-n1c(C=Cc2ccccc2)nc2ccccc21
Reaction #79148
titled compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
N#Cc1cccnc1-n1cc(-c2ccc(Oc3ccccc3)cc2)c2c(N)ncnc21
Reaction #79787
2-[4-amino-5-(4-phenoxyphenyl)-7H-pyrrolo[2,3-d]pyrimidin-7-yl]pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CO[C@@H]1CN(CCCCNc2ncccc2C#N)CC[C@@H]1NC(=O)c1cc(Cl)c(N)c2c1OCC2.CO[C@@H]1CN(CCCCNc2ncccc2C#N)CC[C@@H]1NC(=O)c1cc(Cl)c(N)c2c1OCC2.O
Reaction #80307
cis-4-amino-5-chloro-N-[1-[4-[(3-cyano-2-pyridinyl)-amino]butyl]-3-methoxy-4-piperidinyl]-2,3-dihydro-7-benzofurancarboxamide hemihydrate
수율 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
CO[C@@H]1CN(CCCCNc2ncccc2C#N)CC[C@@H]1NC(=O)c1cc(Cl)c(N)c2c1OCC2.CO[C@@H]1CN(CCCCNc2ncccc2C#N)CC[C@@H]1NC(=O)c1cc(Cl)c(N)c2c1OCC2.O
Reaction #80951
cis-4-amino-5-chloro-N-[1-[4-[(3-cyano-2-pyridinyl)amino ]butyl]-3-methoxy-4-piperidinyl]-2,3-dihydro-7-benzofurancarboxamide hemihydrate
수율 35.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
O=Cc1cccnc1Cl
Reaction #83797
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Cc1ccc(-n2nccn2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncccc2C#N)c1
Reaction #89295
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Cc1ccc(-c2cnn(C)c2)c(C(=O)N2CCC[C@@H](C)[C@H]2CNc2ncccc2C#N)c1
Reaction #89298
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=C(c1ccccc1)c1cccnc1Cl
Reaction #93808
3-benzoyl-2-chloro-pyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1986_09
CCNc1ncccc1C#N
Reaction #96230
2-ethylaminonicotinonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CC(C)(C)OC(=O)N1CCN(Cc2cccc(Oc3ncccc3C#N)c2)CC1
Reaction #173987
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cccnc1SCc1ccccc1
Reaction #174367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cccnc1N1CCC(S(=O)(=O)c2ccc3ccccc3c2)CC1
Reaction #178647
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc(CNc2ncccc2C#N)cc1
Reaction #184024
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1cccnc1NCc1ccc(F)cc1
Reaction #184986
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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