Substructure Search

1336071

CN1CCC(C(=O)c2cccc(NC(=O)c3ccc(F)cc3C(F)(F)F)n2)CC1.Cl
Reaction #58487
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(F)cc3C(F)(F)F)n2)nc1
Reaction #60162
{4-[4-fluoro-2-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}{2-[(5-nitro(2-pyridyl))amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1
O=[N+]([O-])c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(F)cc3C(F)(F)F)n2)nc1
Reaction #60163
{4-[4-fluoro-2-(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(F)cc3C(F)(F)F)n2)nc1
Reaction #60168
6-{[2-({4-[4-fluoro-2-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}amino)ethyl]amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc(-c2nc(NCCNc3ccc(C(F)(F)F)cn3)ncc2-c2ncc[nH]2)c(C(F)(F)F)c1
Reaction #60169
{4-[4-fluoro-2-(trifluoromethyl)phenyl]-5-imidazol-2-ylpyrimidin-2-yl}(2-{[5-(trifluoromethyl)(2-pyridyl)]amino}ethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2c(c1)B(O)OC2C1CCCC1)c1ccc(F)cc1C(F)(F)F
Reaction #88822
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC(C)CC1OB(O)c2cc(NC(=O)c3ccc(F)cc3C(F)(F)F)ccc21
Reaction #88825
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)OB(O)c2cc(NC(=O)c3ccc(F)cc3C(F)(F)F)ccc21
Reaction #88832
4-fluoro-N-(1-hydroxy-3,3-dimethyl-1,3-dihydro-benzo[c][1,2]oxaborol-6-yl)-2-trifluoromethyl benzamide
Yield 113.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2c(c1)B(O)OC2)c1ccc(F)cc1C(F)(F)F
Reaction #88846
4-Fluoro-N-(1-hydroxy-1,3-dihydro-benzo[c][1,2]oxaborol-6-yl)-2-trifluoromethyl-benzamide
Yield 57.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Cl)c1ccc(F)cc1C(F)(F)F
Reaction #182721
DOI: 10.1039/C8SC04228D
Cc1ccn(-c2ccc(C(=O)N3Cc4cccnc4Oc4ccccc43)c(C(F)(F)F)c2)n1
Reaction #210786
DOI: 10.1039/C8SC04228D
COc1ccc(N(C(=O)c2ccc(F)cc2C(F)(F)F)c2ccc(OC)cc2)cc1
Reaction #246507
DOI: 10.1039/C8SC04228D
CCOC(=O)c1c(NC(=O)c2ccc(F)cc2C(F)(F)F)sc2c1C(C)(C)OC2(C)C
Reaction #378405
DOI: 10.1039/C8SC04228D
O=C(c1ccc(F)cc1C(F)(F)F)N1Cc2cccnc2Nc2ccccc21
Reaction #397223
DOI: 10.1039/C8SC04228D
COC(=O)[C@H](C(C)C)N1Cc2ccc(-c3ccc(NC(=O)c4ccc(F)cc4C(F)(F)F)cc3)cc2C1=O
Reaction #491025
compound
Yield 64.0%DOI: 10.6084/m9.figshare.5104873.v1
CN1CCC(C(=O)c2cccc(NC(=O)c3ccc(F)cc3C(F)(F)F)n2)CC1.Cl
Reaction #491411
title compound
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2c(c1)B(O)OCC2)c1ccc(F)cc1C(F)(F)F
Reaction #555182
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CC1(C)Cc2ccc(NC(=O)c3ccc(F)cc3C(F)(F)F)cc2B(O)O1
Reaction #555189
title compound
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)CNC(=O)c1ccc(F)cc1C(F)(F)F
Reaction #593667
Ethyl (4-fluoro-2-trifluoromethylbenzoylamino)acetate
DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccn(-c2ccc(C(=O)N3Cc4cccnc4Nc4ccccc43)c(C(F)(F)F)c2)n1
Reaction #723553
title compound
Yield 33.1%DOI: 10.6084/m9.figshare.5104873.v1
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