#8632483

COC(=O)c1cc(Cl)ccc1N=Cc1cccc(Br)c1
Reaction #203266
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COC(=O)c1cc(Cl)ccc1NS(=O)(=O)c1cccc2nsnc12
Reaction #381184
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CNc1ccc(Cl)cc1C(=O)OC
Reaction #383540
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1cc(Cl)ccc1NC(=O)c1cc(OC)c(OC)c(OC)c1
Reaction #408871
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
COC(=O)c1cc(Cl)ccc1NC1CCCCC1
Reaction #513145
methyl 5-chloro-2-(cyclohexylamino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_01
COC(=O)c1cc(Cl)ccc1NC(=O)OCc1ccccc1
Reaction #535296
2-benzyloxycarbonylamino-5-chloro-benzoic acid methyl ester
Yield 70.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_07
CCCCC(=O)Nc1ccc(Cl)cc1C(=O)OC
Reaction #740889
crystals
Yield 61.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1992_07
COC(=O)c1cc(Cl)cc(I)c1N
Reaction #749453
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cc(Cl)ccc1NC(=O)CN(C)CC(=O)O
Reaction #754463
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cc(Cl)ccc1NC1CCCCC1
Reaction #769812
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (3/10)
COC(=O)c1cc(Cl)ccc1NS(=O)(=O)c1ccc(C)cc1
Reaction #915530
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
CCCCC(=O)Nc1ccc(Cl)cc1C(=O)OC
Reaction #915694
DOI: 10.1039/C8SC04228DTest data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1cc(Cl)ccc1NC(=O)COCC(=O)O
Reaction #1021446
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1cc(Cl)ccc1N=Cc1cccc([N+](=O)[O-])c1
Reaction #1044861
DOI: 10.1039/C8SC04228DValidation data from https://doi.org/10.1039/C8SC04228D
COC(=O)c1cc(Cl)ccc1NS(=O)(=O)c1ccccc1
Reaction #1093705
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
COC(=O)c1cc(Cl)ccc1NC(=O)c1ccc(Cl)nc1
Reaction #1094393
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_09
COC(=O)c1cc(Cl)cc2c1NC(c1cccc(Br)c1)CC2(C)C
Reaction #1124047
2-(3-bromo-phenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline-8-carboxylic acid methyl ester
Yield 21.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
—
Reaction #1182193
intermediate
Yield 90.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_03
COC(=O)c1cc(Cl)ccc1N=Cc1cccc(Br)c1
Reaction #1206151
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
COC(=O)c1cc(Cl)ccc1NC(C)C
Reaction #1209260
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
Page 1Next