Substructure Search

17870

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Reaction #7565
hydrochloride salt
Yield 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Nc1nc2cc(C(F)(F)F)ccc2[nH]1
Reaction #9679
N-(4-Bromo-2-fluorophenyl)-N-[5-(trifluoromethyl)-1H-benzimidazol-2-yl]amine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nc(Nc3ccc(Br)cc3F)sc2c1
Reaction #9682
desired product
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44184
clean desired product
Yield 89.0%DOI: 10.6084/m9.figshare.5104873.v1
C=COCCONC(=O)c1cn(C)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #44185
clean desired product
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)NOCCO)c(Nc2ccc(Br)cc2F)cc1=O
Reaction #44186
clean desired product
Yield 76.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1cc(C(=O)NO)c(Nc2ccc(Br)cc2F)c(F)c1=O
Reaction #44189
desired product
Yield 33.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Nc2ccc(Br)cc2F)c(C(=O)NO)cn(C)c1=O
Reaction #44191
4-(4-Bromo-2-fluorophenylamino)-1,5-dimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid hydroxyamide
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1cnc(OC)c(F)c1Nc1ccc(Br)cc1F
Reaction #44194
4-(4-bromo-2-fluorophenylamino)-5-fluoro-6-methoxy-nicotinic acid methyl ester
DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1c[nH]c(=O)c(F)c1Nc1ccc(Br)cc1F
Reaction #44195
clean desired product
Yield 97.1%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Nc2ccc(Br)cc2F)c(-c2nnn[nH]2)cn(C)c1=O
Reaction #44202
desired product
Yield 77.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(Nc2ccc(Br)cc2F)c(C(=O)NS(=O)(=O)Cc2ccccc2)cn(C)c1=O
Reaction #44206
clean desired product
Yield 68.0%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)c1nn(-c2ccccc2)c(=O)cc1Nc1ccc(Br)cc1F
Reaction #44215
desired product
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1c(Nc2ccc(Br)cc2F)c(C(=O)NOCCO)ccc1=O
Reaction #44219
pure desired product
Yield 60.0%DOI: 10.6084/m9.figshare.5104873.v1
Cn1nc(C(=O)NOCC2CC2)c(Nc2ccc(Br)cc2F)c(Br)c1=O
Reaction #44241
title compound
Yield 40.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1c(N)c(F)c(-c2ccccc2)c(Br)c1C#N
Reaction #45802
compound
Yield 89.5%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Nc1nc2cc(C(F)(F)F)ccc2[nH]1
Reaction #59176
N-(4-Bromo-2-fluorophenyl)-N-[5-(trifluoromethyl)-1H-benzimidazol-2-yl]amine
DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Nc1nc2ccc(OC(F)(F)F)cc2s1
Reaction #59179
product
Yield 58.1%DOI: 10.6084/m9.figshare.5104873.v1
Fc1ccc2nc(Nc3ccc(Br)cc3F)sc2c1
Reaction #59180
desired product
Yield 78.0%DOI: 10.6084/m9.figshare.5104873.v1
Fc1cc(Br)ccc1Nc1nc2cc(C(F)(F)F)ccc2o1
Reaction #59184
title compound
Yield 18.0%DOI: 10.6084/m9.figshare.5104873.v1
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