ethyl 7-nitro-1H-indole-2-carboxylate

NC(=O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #317749
7-nitro-1H-indole-2-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
NC(=O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #368279
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
Reaction #373403
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #423653
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
CCOC(=O)Cn1c(C(=O)OCC)cc2cccc([N+](=O)[O-])c21
Reaction #442870
ethyl 1-ethoxycarbonylmethyl-7-nitro-1H-indole-2-carboxylate
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1998_11
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
Reaction #591791
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_08
CCOC(=O)Cn1c(C(=O)OCC)cc2cccc([N+](=O)[O-])c21
Reaction #737231
ethyl 1-ethoxycarbonylmethyl-7-nitro-1H-indole-2-carboxylate
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
O=C(O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #1133043
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_10
O=C(O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #1301210
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
O=C(O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #1602448
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_07
CCOC(=O)Cn1c(C(=O)OCC)cc2cccc([N+](=O)[O-])c21
Reaction #1643918
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (1/10)
CCOC(=O)Cn1c(C(=O)OCC)cc2cccc([N+](=O)[O-])c21
Reaction #1687791
ethyl 1-ethoxycarbonylmethyl-7-nitro-1H-indole-2-carboxylate
収率 78.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_11
O=C(O)c1cc2cccc([N+](=O)[O-])c2[nH]1
Reaction #1889992
7-nitro-1H-indole-2-carboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
O=C(O)c1cc2cccc(NC3CCOCC3)c2[nH]1
Reaction #1889993
title compound
収率 76.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_01
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
Reaction #1938537
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2015_02
CCOC(=O)c1cc2cccc(N)c2[nH]1
Reaction #1962001
title compound
収率 528.8%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_11
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
Reaction #2047417
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_04
CCOC(=O)c1cc2cccc([N+](=O)[O-])c2n1COC
Reaction #2081846
title compound
収率 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_01