Recherche de Sous-structure

18200

O=C(Nc1cc(Br)cnc1O)c1ccc(C(F)(F)F)cc1
Reaction #7901
title compound
Rendement 60.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc(C(F)(F)F)cc4)c3C2=O)C(=O)N1
Reaction #10104
N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-4-trifluoromethyl-benzamide
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Nc2cncc(-c3ccc(C(=O)c4ccc(C(F)(F)F)cc4)cc3N)n2)cc(OC)c1OC
Reaction #44594
title compound
Rendement 46.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)Cl
Reaction #49105
2-Methyl-4,6-bis(trifluoromethyl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)Cl
Reaction #49106
2-(methylthio)-4,6-bis(trifluoromethyl)benzoyl chloride
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)Cl
Reaction #49113
title product
Rendement 109.3%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)NC(c1ccccc1)C(C)(C)N1CCCC1
Reaction #49126
title product
Rendement 54.0%DOI: 10.6084/m9.figshare.5104873.v1
CSc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)NC(c1ccccc1)C(C)(C)N1CCCC1
Reaction #49129
title product
Rendement 85.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1C(=O)NC(c1ccccc1)C1(N(C)C)CCCC1
Reaction #49130
title product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #54529
colorless needles
Rendement 77.0%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #56968
solid
Rendement 63.0%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)c1ccc(OCCO/N=C/c2ccc(C(C)(C)C)cc2)cc1OC(=O)c1ccc(C(F)(F)F)cc1
Reaction #57928
4-{2-[({(E)-[4-(tert-butyl)phenyl]methylidene}amino)oxy]ethoxy}-2-{[4-(trifluoromethyl)benzoyl]oxy}benzoic acid tert-butyl ester
Rendement 96.1%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3)n2)nc1
Reaction #60153
{5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}{2-[(5-nitro(2-pyridyl))amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3)n2)nc1
Reaction #60154
6-{[2-({5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)ethyl]-amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
FC(F)(F)c1ccc(-c2nc(NCCNc3ccc(C(F)(F)F)cn3)ncc2-c2ncc[nH]2)cc1
Reaction #60155
{5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}(2-{[5-(trifluoromethyl)(2-pyridyl)]amino}ethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3F)n2)nc1
Reaction #60165
{4-[2-fluoro-4-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}{2-[(5-nitro(2-pyridyl))amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3F)n2)nc1
Reaction #60175
6-{[2-({4-[2-fluoro-4-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}amino)ethyl]amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
O=c1nncc2c3c(cccc13)N=C2c1ccc(C(F)(F)F)cc1
Reaction #61625
4-trifluoromethylphenyl-[1,2]diazepino[4,5,6-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(F)(F)F)cc(OC)c1C(=O)Cl
Reaction #67709
title compound
Rendement 98.9%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(C(F)(F)F)cc(OC)c1C(=O)NC(C)(C)CO
Reaction #67710
title compound
Rendement 94.7%DOI: 10.6084/m9.figshare.5104873.v1
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