2-aminobenzonitrile

COc1ccc(S(=O)(=O)Nc2ccccc2C#N)cc1
Reaction #2508
title compound
Rendimiento 63.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)/C=C(\Nc1ccccc1C#N)C(=O)OC
Reaction #3214
solid
Rendimiento 44.3%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COC(=O)CNc1ccccc1C#N
Reaction #3661
methyl [N-(2-cyanophenyl)amino]acetate
Rendimiento 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
N#Cc1ccccc1NC1=CC(=O)CCC1
Reaction #6316
2-(3-oxocyclohexen-1-yl)aminobenzonitrile
Rendimiento 93.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1c2c(nc3ccccc13)CCCC2.O
Reaction #6317
9-amino-1,2,3,4-tetrahydroacridine hydrate
Rendimiento 67.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1993_09
Nc1ccccc1C(=O)C1CCCC1
Reaction #58586
crude product
Rendimiento 93.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccccc1NC(=S)NC(=O)c1ccccc1
Reaction #72613
N-(2-Cyanophenylcarbamothioyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
N#Cc1ccccc1NC(=O)NC(=O)c1ccccc1
Reaction #72625
N-(2-Cyanophenylcarbamoyl)benzamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
NC1=NS(=O)(=O)Nc2ccccc21
Reaction #72638
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ccccc1-c1nnn[nH]1
Reaction #77694
pure product
Rendimiento 65.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
CCOP(=O)(Cc1ccc(C(=O)Nc2ccccc2C#N)cc1)OCC
Reaction #83176
diethyl 4-[N-(2-cyanophenyl)carbamoyl]benzyl-phosphonate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
COC(=O)CNc1ccccc1C#N
Reaction #83482
methyl [N-(2-cyanophenyl)amino]acetate
Rendimiento 80.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
N#Cc1ccccc1Nc1cc(Cl)ncc1Cl
Reaction #90770
2-[(2,5-Dichloro-4-pyridinyl)amino]benzonitrile
Rendimiento 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
N#Cc1cc(Cl)ccc1N
Reaction #177367
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccccc1N=CN1CCNC1=N[N+](=O)[O-]
Reaction #202229
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccccc1C(=O)c1ccc(F)cc1
Reaction #212055
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Nc1ccccc1C(=O)c1cccc(F)c1
Reaction #220442
2-Amino-3′-fluorobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
Nc1ccccc1C(=O)c1ccc(F)cc1
Reaction #220443
2-Amino-4′-fluorobenzophenone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_06
CN1CCC(C(=O)c2ccccc2N)CC1
Reaction #221382
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Nc1ccccc1C(=O)C1CCCC1
Reaction #237322
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Página 1Siguiente