5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine

O=C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #1435
1-(4-nitrobenzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin-5-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
COc1ccccc1-c1ccc(C(=O)N2CCCC(=O)c3ccccc32)cc1
Reaction #1445
1-(2'-methoxybiphen-4-ylcarbonyl)-5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_03
O=C1CCCN(C(=O)c2ccccc2)c2ccccc21
Reaction #172955
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCN(C(=O)c2ccc([N+](=O)[O-])cc2)c2ccccc21
Reaction #190456
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C1CCCNc2ccccc21
Reaction #307960
title compound
المردود 79.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C1CCCN(C(=O)c2ccccc2)c2ccccc21
Reaction #307961
title compound
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1ccc2c(c1)Nc1c(cnn1C)CN2C(=O)c1ccc(CN)c(C)c1
Reaction #308140
title compound
المردود 35.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cl.Cn1ncc2c1Nc1cc(Cl)ccc1N(C(=O)c1ccc(CN)c(F)c1)C2
Reaction #308143
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cl.Cn1ncc2c1Nc1cc(Cl)ccc1N(C(=O)c1ccc(CN)c(Cl)c1)C2
Reaction #308149
title compound
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cc1nc2c([nH]1)-c1ccccc1N(C(=O)c1ccc(CNC(=O)C3CC3)c(C)c1)CC2
Reaction #308173
title compound
المردود 53.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
CC(C)OC(=O)N1CCCC(=O)c2ccccc21
Reaction #384708
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C1CCCNc2ccccc21
Reaction #394800
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COc1ccccc1-c1ccc(C(=O)N2CCCC(=O)c3ccccc32)cc1
Reaction #429492
1-(2'-methoxybiphen-4-ylcarbonyl)-5-oxo-2,3,4,5-tetrahydro-1H-1-benzazepine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
CO/N=C1/CCNCc2ccccc21
Reaction #627141
desired product
المردود 67.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_10
O=C1CCCN(C(=O)CSc2nc3ccccc3s2)c2ccccc21
Reaction #759288
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
c1ccc2c(c1)CCCCN2
Reaction #911786
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
Cc1ccc(S(=O)(=O)N2CCCC(=O)c3ccccc32)cc1
Reaction #1297161
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
c1ccc2c(c1)CCCCN2
Reaction #1492085
compound 6
المردود 47.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=C1CCCN(C(=O)CSc2nc3ccccc3s2)c2ccccc21
Reaction #1492107
37
المردود 29.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
O=C1CCCNc2ccccc21
Reaction #1492129
compound 5
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_12
الصفحة 1التالي