Substructure Search

Cl.N=C(N)c1ccc(F)cc1

CCCCCCC(=O)N(C)C1N(C)C(c2ccc(N3CCCCC3)cc2)=NC1(C(F)(F)F)C(F)(F)F.Cl
Reaction #50582
title compound
Yield 22.4%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c(NC(=N)c2ccc(F)c(Cl)c2)c1
Reaction #173490
DOI: 10.1039/C8SC04228D
NC(=NO)c1ccc(F)c(Cl)c1
Reaction #245676
DOI: 10.1039/C8SC04228D
CCOC(=O)c1cnc(-c2ccc(F)cc2)nc1C
Reaction #306837
ethyl-2-(4-fluorophenyl)-4-methyl-pyrimidine-5-carboxylate
Yield 88.5%DOI: 10.6084/m9.figshare.5104873.v1
CCc1cnc(-c2ccc(F)c(F)c2)nc1
Reaction #322769
5-ethyl-2-(3,4-difluorophenyl)pyrimidine
Yield 106.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cnc(-c2ccc(F)cc2)nc1-c1cccc(C(F)(F)F)c1
Reaction #413998
2-(4-fluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine
Yield 81.1%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1cnc(-c2ccc(F)cc2F)nc1-c1cccc(C(F)(F)F)c1
Reaction #413999
2-(2,4-difluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine
Yield 77.5%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c(NC(=N)c2ccc(F)cc2Cl)c1
Reaction #436673
title compound
Yield 72.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c2[nH]c(-c3ccc(F)cc3Cl)nc12
Reaction #436674
title compound
Yield 52.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c(NC(=N)c2ccc(F)c(Cl)c2)c1
Reaction #436678
title compound
Yield 45.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c2[nH]c(-c3ccc(F)c(Cl)c3)nc12
Reaction #436679
title compound
Yield 30.0%DOI: 10.6084/m9.figshare.5104873.v1
N=C(NS(=O)(=O)c1ccc(F)c(Cl)c1)c1ccc(F)c(Cl)c1
Reaction #438311
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=NC(C)(C)CN2C(c2nc3cc(Cl)ccc3c(=O)n2Cc2ccccc2)C(C)C)ccc1F
Reaction #577441
(±)-3-benzyl-7-chloro-2-{1-[2-(4-fluoro-3-methyl-phenyl)-4,4-dimethyl-4,5-dihydro-imidazol-1-yl]-2-methyl-propyl}-3H-quinazolin-4-one
Yield 43.0%DOI: 10.6084/m9.figshare.5104873.v1
COC(=O)c1ccc(OC)c(NC(=N)c2ccc(F)cc2Cl)c1
Reaction #759260
DOI: 10.1039/C8SC04228D
NCc1c(N)nc(-c2ccc(F)cc2Cl)nc1-c1ccc(Cl)cc1Cl
Reaction #1071047
title compound
DOI: 10.6084/m9.figshare.5104873.v1
O=S1ON=C(c2ccc(F)cc2)N1c1ccc(Cl)cc1Cl
Reaction #1120901
3-(2,4-dichlorophenyl)-4-(4-fluorophenyl)-1,2,3,5-oxathiadiazole-2-oxide
DOI: 10.6084/m9.figshare.5104873.v1
CC1CCCCN1C1=NC(=N)C(=C2NC(=N)c3c(F)c(F)c(Cl)c(F)c32)S1.Cl
Reaction #1199728
1-imino-5-chloro-4,6,7-trifluoro-3-[2-(2-methylpiperidino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(C2=NC(C)(C)CN2C(c2nc3cc(Cl)ccc3c(=O)n2Cc2ccccc2)C(C)C)ccc1F
Reaction #1212950
DOI: 10.1039/C8SC04228D
N=C(NS(=O)(=O)c1ccc(F)c(Cl)c1)c1ccc(F)c(Cl)c1
Reaction #1229319
DOI: 10.1039/C8SC04228D
CCS(=O)(=O)N(C/C=C/c1cc(C(=N)N)ccc1F)c1ccc(OC2CCN(C(C)=N)CC2)cc1.Cl.Cl
Reaction #1355340
title compound
Yield 144.3%DOI: 10.6084/m9.figshare.5104873.v1
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