Recherche de Sous-structure

1417447

CCOC(=O)C(=CN(c1cc(N2CCNCC2)c(F)c(C)c1[N+](=O)[O-])C1CC1)C(=O)OCC
Reaction #1387
diethyl [N-cyclopropyl-N-[3-(1-piperazinyl)-4-fluoro-5-methyl-6-nitrophenyl]amino-methylene]malonate
DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)CCCOc1ccc([N+](=O)[O-])cc1F
Reaction #11615
Diethyl-[3-(2-fluoro-4-nitro-phenoxy)-propyl]-amine
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(OCc2ccccc2)c(F)c1
Reaction #41601
4-benzyloxy-3-fluoroaniline
DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(-c2cc(Oc3ccccc3OCc3ccccc3)c([N+](=O)[O-])cc2F)c1=O
Reaction #43650
2-(2-benzyloxyphenoxy)-5-fluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]nitrobenzene
Rendement 80.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(C(F)(F)F)cc(=O)n(-c2cc(Oc3ccccc3OCc3ccccc3)c(N)cc2F)c1=O
Reaction #43651
2-(2-benzyloxyphenoxy)-5-fluoro-4-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-1,2,3,6-tetrahydropyrimidin-1-yl]aniline
Rendement 79.6%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(F)ccc1Oc1ccccc1
Reaction #44426
title compound
Rendement 86.0%DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OC(=O)c2ccc(C(c3c(F)cc([N+](=O)[O-])cc3F)n3cncn3)cc21
Reaction #50336
5-[(2,6-difluoro- 4-nitrophenyl)-[1,2,4]triazol-1-yl-methyl]-3,3-dimethyl-3H-isobenzofuran-1-one
Rendement 67.4%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2cc3cc(F)c(F)cc3[nH]2)cc1N
Reaction #53769
5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenylamine
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])c(N)c(F)c1Nc1ccccc1C
Reaction #60241
clean desired product
Rendement 68.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc2nc[nH]c2c(F)c1Nc1ccccc1C
Reaction #60242
7-Fluoro-6-o-tolylamino-1H-benzoimidazole-5-carboxylic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])c(N)c(F)c1Nc1ccccc1F
Reaction #60250
pure desired product
Rendement 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc([N+](=O)[O-])c(N)c(F)c1Nc1ccccc1Cl
Reaction #60254
pure desired product
Rendement 12.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cc(N)c(N)c(F)c1Nc1ccccc1Cl
Reaction #60255
pure desired product
Rendement 48.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2c(c1)nc(/C=C/c1ccccc1)n2-c1ccccn1
Reaction #79198
titled compound
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #81976
orange crystalline solid
Rendement 69.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #81994
brown solid
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Br)cc(F)cc1[N+](=O)[O-]
Reaction #82003
6-Bromo-4-fluoro-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82564
orange crystalline solid
Rendement 69.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #82582
brown solid
Rendement 84.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1c(Br)cc(F)cc1[N+](=O)[O-]
Reaction #82591
6-Bromo-4-fluoro-2-nitroaniline
DOI: 10.6084/m9.figshare.5104873.v1
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