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C1=CC=C(C(=C1)N)F

Cc1c(Nc2ccc(Br)cc2F)c(C(=O)NS(=O)(=O)Cc2ccccc2)cn(C)c1=O
Reaction #44206
clean desired product
Ausbeute 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc([N+](=O)[O-])c(F)c1)N1CCCC1
Reaction #46884
(3-Fluoro-4-nitro-phenyl)-pyrrolidin-1-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(C(=O)N2CCCC2)cc1F
Reaction #46885
(4-Amino-3-fluoro-phenyl)-pyrrolidin-1-yl-methanone
DOI: 10.6084/m9.figshare.5104873.v1
CC(=NNc1ccc(F)cc1F)C(=O)O
Reaction #62527
2-(2,4-difluorophenylhydrazono)propionic acid
Ausbeute 943.2%DOI: 10.6084/m9.figshare.5104873.v1
CCN[C@@H]1CN(c2c(F)cc3c(=O)c(C(=O)O)cn(C4CC4)c3c2Cl)C[C@H]1SC
Reaction #64995
8-chloro-1-cyclopropyl-7-(trans-3-ethylamino-4-methylthio-1-pyrrolidinyl)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(F)c([N+](=O)[O-])c1
Reaction #65071
objective product
Ausbeute 93.0%DOI: 10.6084/m9.figshare.5104873.v1
CCS(=O)(=O)Nc1ccc(F)c(N)c1
Reaction #65072
objective product
Ausbeute 89.2%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNC(=O)c1n[nH]c2ccccc12)c1ccncc1Nc1ccc(I)cc1F
Reaction #67812
N′-{3-[(2-fluoro-4-iodophenyl)amino]isonicotinoyl}-1H-indazole-3-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNc1ccnc2cc(Cl)ccc12)c1ccncc1Nc1ccc(I)cc1F
Reaction #67837
N′-(7-chloroquinolin-4-yl)-3-[(2-fluoro-4-iodophenyl)amino]isonicotino-hydrazide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(F)cc(C(F)(F)F)c1)c1ccncc1Nc1ccc(I)cc1F
Reaction #67870
3-[(2-fluoro-4-iodophenyl)amino]-N-[3-fluoro-5-(trifluoromethyl)benzyl]isonicotinamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(NN=CC(=O)C(F)(F)F)c(F)cc1Cl
Reaction #76761
3,3,3-trifluoro-2-oxo-propanal 1-(4-chloro-2-fluoro-5-isopropoxyphenylhydrazone)
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)Oc1cc(NN=CC(=O)C(F)(F)F)c(F)cc1Br
Reaction #76768
3,3,3-trifluoro-2-oxopropanal 1-(4-bromo-2-fluoro-5-isopropoxyphenylhydrazone)
Ausbeute 67.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)Nc1cc(N)ccc1F
Reaction #84402
title compound
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(NC(=O)OC(C)(C)C)c1ccc(N)c([N+](=O)[O-])c1
Reaction #86486
title compound
Ausbeute 76.4%DOI: 10.6084/m9.figshare.5104873.v1
O=C(c1ccc(-n2cnnn2)c(F)c1)N(C1CC1)C1CCN(c2ncc(Cl)cn2)CC1
Reaction #156092
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1cc(-c2nc3ccccc3o2)cc(C(F)(F)F)c1F
Reaction #161458
title compound
Ausbeute 54.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162316
desired product
Ausbeute 65.0%DOI: 10.6084/m9.figshare.5104873.v1
C[C@@H](Nc1cc(N2CCN(C(=O)[C@H]3CCCCN3)CC2)ccc1F)c1ccc(Cl)cc1Cl
Reaction #162317
title compound
Ausbeute 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)C(Nc1cc(F)ccc1F)c1ccccc1
Reaction #164175
solid
Ausbeute 67.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NNC(=O)c1n[nH]c2ccccc12)c1ccncc1Nc1ccc(I)cc1F
Reaction #165977
N′-{3-[(2-fluoro-4-iodophenyl)amino]isonicotinoyl}-1H-indazole-3-carbohydrazide
DOI: 10.6084/m9.figshare.5104873.v1
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