p-aminobenzonitrile

N#Cc1ccc(Nc2ccc(C(=O)NC3CCCCC3)cn2)cc1
Reaction #169
المردود 9.9%750 AstraZeneca ELN dataset
N#Cc1ccc(NCC(O)CO)cc1
Reaction #1125
p-(N-2,3-dihydroxypropylamino)benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(NC(=O)c2ccccc2SSc2ccccc2C(=O)Nc2ccc(C#N)cc2)cc1
Reaction #3821
title compound
المردود 12.5%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccc(N2C=CC(N)=C([N+](=O)[O-])C2)cc1
Reaction #6451
N-(4-cyanophenyl)-4-amino-3-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
N#Cc1ccc2nc(N)sc2c1
Reaction #9196
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc2nc(N)sc2c1
Reaction #9198
title compound
المردود 67.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#CCc1ccc2nc(N)sc2c1
Reaction #9263
(2-Amino-1,3-benzothiazol-6-yl)methyl cyanide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
N#Cc1ccc(Nc2cc(Cl)nc(N)n2)cc1
Reaction #44703
4-[(2-Amino-6-chloropyrimidin-4-yl)amino]benzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N#Cc1ccc(N/C(=C2\C(=O)Nc3ccccc32)c2ccccc2)cc1
Reaction #53057
(Z)-3-[1-(4-cyanophenylamino)-1-phenyl-methylidene]-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#Cc1ccc(N/C(=C2\C(=O)Nc3ccc([N+](=O)[O-])cc32)c2ccccc2)cc1
Reaction #53081
(Z)-3-[1-(4-cyanophenylamino)-1-phenyl-methylidene]-5-nitro-2-indolinone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
N#Cc1ccc(Nc2nc(Cl)nc(Cc3c(Cl)cccc3Cl)n2)cc1
Reaction #53322
4-[[4-chloro-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]-amino]benzonitrile
المردود 104.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2005_02
Cc1ccc(Cl)cc1-c1cc(Nc2ccc(C#N)cc2)nc(N)n1
Reaction #56823
title compound
المردود 71.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CCOc1ccc(Cl)cc1-c1cc(Nc2ccc(C#N)cc2)nc(N)n1
Reaction #56852
title compound
المردود 74.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1ccc(Br)cc1-c1cc(Nc2ccc(C#N)cc2)nc(N)n1
Reaction #56880
title compound
المردود 72.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(NC(=O)C(F)(F)C(F)(F)C(F)(F)F)cc1
Reaction #63298
2,2,3,3,4,4,4-heptafluoro-N-[4-(cyano)phenyl]butanamide
المردود 36.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1988_08
N#Cc1ccc(Nc2nc(N)c(Cl)c(Cl)n2)cc1
Reaction #69645
4-[(4-amino-5,6-dichloro-2-pyrimidinyl)amino]benzonitrile
المردود 6.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Cc1cc(C)c(Nc2nc(Nc3ccc(C#N)cc3)ncc2Br)c(C)c1
Reaction #69646
4-[[5-bromo-4-[(2,4,6-trimethylphenyl)amino]-2-pyrimidinyl]amino]benzonitrile
المردود 13.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
CSC1C(=O)Nc2ccc(C#N)cc21
Reaction #72553
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1ccc(Nc2nnc(Cc3ccncc3)c3ccccc23)cc1
Reaction #78149
Title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOC(=O)CCN(C(=O)c1cnc2sc(CNc3ccc(C#N)cc3)nc2c1)c1ccccc1
Reaction #78616
crude product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
الصفحة 1التالي