Substructure Search

445827

O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C(F)(F)F
Reaction #87629
desired title product
Yield 41.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)cc1CNC(=O)C(F)(F)F
Reaction #87650
desired product
Yield 24.5%DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2cc(S(=O)(=O)NC3CC3)ccc2Cl)nn1-c1ccc(C(F)(F)F)cc1
Reaction #87782
desired product
Yield 60.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C(F)(F)F
Reaction #87785
desired product
Yield 41.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)C(F)(F)F)c(C)c1-c1nn(-c2ccc(C(F)(F)F)cc2)c(=O)[nH]1
Reaction #87791
desired product
Yield 45.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c(Cl)cc1F)C(F)(F)F
Reaction #87798
desired product
Yield 6.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(C(F)F)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #87843
desired product
Yield 22.8%DOI: 10.6084/m9.figshare.5104873.v1
CC(C)(C)OC(=O)NNc1ccc(C(F)(F)F)cc1C(=O)/N=c1\sc(C(C)(C)C)cn1C[C@H]1CCCO1
Reaction #169948
title compound
Yield 15.7%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C(F)(F)F
Reaction #596026
desired title product
Yield 41.5%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)cc1CNC(=O)C(F)(F)F
Reaction #596046
desired product
Yield 24.5%DOI: 10.6084/m9.figshare.5104873.v1
—
Reaction #596172
pure product
DOI: 10.6084/m9.figshare.5104873.v1
O=c1[nH]c(-c2cc(S(=O)(=O)NC3CC3)ccc2Cl)nn1-c1ccc(C(F)(F)F)cc1
Reaction #596182
desired product
Yield 60.5%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1ccc(Cl)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1)C(F)(F)F
Reaction #596185
desired product
Yield 41.5%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(CNC(=O)C(F)(F)F)c(C)c1-c1nn(-c2ccc(C(F)(F)F)cc2)c(=O)[nH]1
Reaction #596192
desired product
Yield 45.9%DOI: 10.6084/m9.figshare.5104873.v1
O=C(NCc1cc(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c(Cl)cc1F)C(F)(F)F
Reaction #596199
desired product
Yield 6.7%DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cnc(C(F)F)c(-c2nn(-c3ccc(C(F)(F)F)cc3)c(=O)[nH]2)c1
Reaction #596245
desired product
Yield 25.3%DOI: 10.6084/m9.figshare.5104873.v1
CN(Nc1ccc(C(F)(F)F)cc1C(F)(F)F)C(=O)OC(C)(C)C
Reaction #1525249
N′-(2,4-bis-trifluoromethyl-phenyl)-N-methyl-hydrazinecarboxylic acid tert-butyl ester
Yield 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c2c(c(=O)n1-c1ccc(C(F)(F)F)cc1C(F)(F)F)[C@H]1CC[C@]2(C)C1(C)C
Reaction #1525250
(4S,7R)-2-(2,4-bis-trifluoromethyl-phenyl)-1,7,8,8-tetramethyl-1,2,4,5,6,7-hexahydro-4,7-methano-indazol-3-one
Yield 66.5%DOI: 10.6084/m9.figshare.5104873.v1
CN(Nc1ccc(C(F)(F)F)cc1C(F)(F)F)C(=O)OC(C)(C)C
Reaction #2410823
DOI: 10.1039/C8SC04228D