An 25 Reaktionen beteiligt

13602

O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #11905
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #77315
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_03
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #173680
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CCOC(=O)c1c(Nc2c([N+](=O)[O-])ccc(Cl)c2Cl)sc2ccccc12
Reaction #266571
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #429374
2,3,4-trichloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #429375
2,3,4-trichloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #702079
2,3,4-Trichloronitrobenzene
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_03
N#Cc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #702080
2,3-Dichloro-6-nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_03
N#Cc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #723542
2,3-dichloro-6-nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
O=[N+]([O-])c1ccc(Cl)c(Cl)c1Cl
Reaction #723547
title product
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
N#Cc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #723548
2,3-Dichloro-6-nitrobenzonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_02
—
Reaction #737109
dihydrate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2001_08
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #929132
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_04
O=C(O)C1CN(C(=O)OCc2ccccc2)CCN1c1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #1103564
desired product
Ausbeute 43.6%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_11
CC(C)CNc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #1162028
2,3-dichloro-6-nitro-N-isobutylaniline
Ausbeute 98.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
Nc1c([N+](=O)[O-])ccc(Oc2ccccc2)c1Cl
Reaction #1162029
2-Chloro-3-phenoxy-6-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1983_07
CC(C)CNc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #1220618
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (7/10)
N#Cc1c([N+](=O)[O-])ccc(Cl)c1Cl
Reaction #1303101
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (5/10)
CCOC(=O)c1c(Nc2c(N)ccc(Cl)c2Cl)sc2ccccc12
Reaction #1368972
ethyl 2-(6-amino-2,3-dichloroanilino)benzo[b]thiophene-3-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2002_09
CN1CCCC1Cc1c[nH]c2ccc(Nc3c([N+](=O)[O-])ccc(Cl)c3Cl)cc12
Reaction #1506343
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_03
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