Busqueda de Subestructura

641878

CCOC(=O)c1c(Cl)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65746
2-Chloro-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c(OC)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OC
Reaction #65748
3,4-Dimethoxycarbonyl-2-methoxy-5-nitro-6-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2ccc(OC)cc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65761
2-Chloro-3,4-diethoxycarbonyl-6-(4-methoxyphenyl)-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2ccc(OC)cc2)c(N)c1C(=O)OCC
Reaction #65762
3-Amino-6-chloro-4,5-diethoxycarbonyl-2-(4-methoxyphenyl)pyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2ccc(O)cc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65767
2-Chloro-3,4-diethoxycarbonyl-6-(4-hydroxyphenyl)-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2cccc(N)c2)c(N)c1C(=O)OCC
Reaction #65773
title compound
Rendimiento 91.3%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65775
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-n2ccnc2)nc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65776
title compound
Rendimiento 89.8%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(-n2cncn2)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65778
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(S(=O)(=O)c2ccc(C)cc2)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65783
title compound
Rendimiento 57.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(-c2ccc(N)cc2)c(N)c1C(=O)OCC
Reaction #65786
title compound
Rendimiento 74.2%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(S(=O)(=O)O)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65788
white crystals
Rendimiento 59.9%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(S(=O)(=O)O)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #209959
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)nc(-c2ccc(OC)cc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #375906
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(S(=O)(=O)c2ccc(C)cc2)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #896880
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #1220480
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)nc(-c2ccc(O)cc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #1318912
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(-n2cncn2)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #1662583
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(Cl)nc(-c2ccccc2)c([N+](=O)[O-])c1C(=O)OCC
Reaction #2412153
DOI: 10.1039/C8SC04228D