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1052285

O=C1OC(=O)c2c1c(Cl)nc1ccccc21
Reaction #5225
4-Chloro-furo[3,4-c]quinoline-1,3-dione
DOI: 10.6084/m9.figshare.5104873.v1
O=C1OCc2c1c(Cl)nc1ccccc21
Reaction #5226
4-Chloro-furo[3,4-c]quinolin-3(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1cnc(-c2ccccc2)c(N)c1C(=O)OCC
Reaction #65742
3-Amino-4,5-diethoxycarbonyl-2-phenylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
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(C)c([N+](=O)[O-])c1C(=O)OCC
Reaction #65754
2-Chloro-3,4-diethoxycarbonyl-6-methyl-5-nitropyridine
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1c(Cl)nc(C)c(N)c1C(=O)OCC
Reaction #65755
3-Amino-6-choro-4,5-diethyoxycarbonyl-2-methylpyridine
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ncc2c(=O)[nH][nH]c(=O)c2c1N
Reaction #65756
8-Amino-7-methylpyrido[3.4-d]pyridazine-1,4(2H,3H)dione
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
COc1ccc(-c2nc(Cl)c3c(=O)[nH][nH]c(=O)c3c2N)cc1
Reaction #65763
8-Amino-5-chloro-7-(4-methoxyphenyl)pyrido[3,4-d]pyridazine-1,4-(2H,3H)dione
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
Nc1cccc(-c2nc(Cl)c3c(=O)[nH][nH]c(=O)c3c2N)c1
Reaction #65774
title compound
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
Nc1ccc(-c2nc(Cl)c3c(=O)[nH][nH]c(=O)c3c2N)cc1
Reaction #65787
title compound
DOI: 10.6084/m9.figshare.5104873.v1
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