2-amino-5-chloropyridine

Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Reaction #40402
(2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc([N+](=O)[O-])c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #40404
N-(5-chloro(2-pyridyl))(5-methyl-2-nitrophenyl)carboxamide
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Reaction #40420
(2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide
المردود 99.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Reaction #40429
(2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide
المردود 100.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Cc1ccc([N+](=O)[O-])c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #40431
N-(5-chloro(2-pyridyl))(5-methyl-2-nitrophenyl)carboxamide
المردود 92.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
Nc1ccc(Cl)cc1C(=O)Nc1ccc(Cl)cn1
Reaction #40448
(2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CCl)Nc1ccc(Cl)cn1
Reaction #44979
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)Nc1ccc(Cl)cn1
Reaction #46787
2-Bromo-N-(5-Chloro-pyridin-2-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(CBr)Nc1ccc(Cl)cn1
Reaction #61523
2-Bromo-N-(5-chloro-pyridin-2-yl)-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
COc1ccc([N+](=O)[O-])c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #67625
2-nitro-N-(5-chloro-pyridin-2-yl)-5-methoxy-benzamide
المردود 88.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
Nc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #81869
2
المردود 56.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1ncc(Cl)cc1[N+](=O)[O-]
Reaction #83783
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1997_04
Nc1ncc(Cl)cc1I
Reaction #86929
5-chloro-3-iodopyridin-2-amine
المردود 64.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
Nc1ncc(Cl)cc1I
Reaction #88504
title compound
المردود 169.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
O=c1[nH]cc(Cl)cc1[N+](=O)[O-]
Reaction #94637
5-chloro-3-nitro-2-pyridone
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1978_12
CCOC(=O)C(=O)Nc1ccc(Cl)cn1
Reaction #186132
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
COc1ccc([N+](=O)[O-])c(C(=O)Nc2ccc(Cl)cn2)c1
Reaction #195270
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)[Si](C)(C)OCCCC(Oc1ncnc2c1cnn2-c1ncccc1Cl)C(=O)Nc1ccc(Cl)cn1
Reaction #196898
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(O)c1nccnc1C(=O)Nc1ccc(Cl)cn1
Reaction #200817
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=C(Nc1ccc(Cl)cn1)c1ccc(Cl)cc1[N+](=O)[O-]
Reaction #211917
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
الصفحة 1التالي