Recherche de Sous-structure

Nc1cccc(C(F)F)c1

Nc1cc(C(F)(F)F)ccc1Oc1ccc2c(c1)CCC(c1ccccc1)O2
Reaction #59506
5-Trifluoromethyl-2-(2-phenylchroman-6-yloxy)-aniline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C(F)(F)F)cc(N)c1Oc1ccc2c(c1)CCC(c1ccccc1)O2
Reaction #59514
3-Amino-5-(trifluoromethyl)-2-(2-phenylchroman-6-yloxy)-aniline
DOI: 10.6084/m9.figshare.5104873.v1
Nc1cc(C(F)(F)F)cc(N)c1Oc1ccc2c(c1)CC(c1ccccc1)C2
Reaction #59525
2-(2-Phenylindan-5-yloxy)-5-trifluoromethylbenzene-1,3-diamine
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1ccc2c(c1)C(F)(F)C(F)(F)O2)N1CC(c2ccccc2)=C(c2ccc(OC(F)F)cc2)N1
Reaction #63971
N-(2,3-dihydro-2,2,3,3-tetrafluorobenzofuran-5-yl)-3-(4-difluoromethoxyphenyl)-4-phenylpyrazoline-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
O=C(Nc1cccc(C(F)(F)F)c1)n1ccc2cc(Oc3ccnc(Cl)n3)ccc21
Reaction #73383
5-(2-chloropyrimidin-4-yloxy)-N-(3-(trifluoromethyl)phenyl)-1H-indole-1-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
CC(=Nc1cc(C(F)(F)F)cc2nc(C)n(C(C)C)c12)c1ccccc1
Reaction #74997
desired product
DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)CC(=O)Nc1ccc(N2CCOCC2)c(C(F)(F)F)c1
Reaction #84512
title compound
Rendement 75.0%DOI: 10.6084/m9.figshare.5104873.v1
C/C(N)=C/C(=O)Nc1ccc(N2CCOCC2)c(C(F)(F)F)c1
Reaction #84513
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(=O)n(-c2ccc(N3CCOCC3)c(C(F)(F)F)c2)c(C)n1
Reaction #84514
title compound
Rendement 70.0%DOI: 10.6084/m9.figshare.5104873.v1
Nc1ccc(F)c(C(F)F)c1
Reaction #87552
desired product
Rendement 80.1%DOI: 10.6084/m9.figshare.5104873.v1
Nc1cccc(C(F)F)c1
Reaction #87553
desired product
Rendement 97.8%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3cc(CNC(=O)C(F)(F)F)ccc3Cl)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)F)c1
Reaction #87577
title compound
DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1ccc(F)c(C(F)F)c1
Reaction #87746
desired product
Rendement 18.6%DOI: 10.6084/m9.figshare.5104873.v1
COc1cc(-n2nc(-c3c(C)cccc3Cl)[nH]c2=O)ccc1C(=O)Nc1cccc(C(F)F)c1
Reaction #87747
desired product
Rendement 26.9%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(NC(=O)Nc3cc(C(F)(F)F)ccc3F)cc2)c2c(N)ncnn2c1CN1CCCOCC1
Reaction #160888
desired product
Rendement 15.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(C)c(CN3CCOCC3)n3ncnc(N)c23)ccc1NC(=O)Nc1cc(C(F)(F)F)ccn1
Reaction #160890
desired product
Rendement 36.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1cc(-c2c(C)c(CN3CCOCC3)n3ncnc(N)c23)ccc1NC(=O)Nc1cc(C(F)(F)F)ccc1F
Reaction #160891
desired product
Rendement 16.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2ccc(NC(=O)Nc3cc(C(F)(F)F)ccn3)cc2)c2c(N)ncnn2c1CN1CCOCC1
Reaction #160892
desired product
Rendement 44.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1c(-c2cc(F)c(NC(=O)Nc3cc(C(F)(F)F)ccc3F)cc2F)c2c(N)ncnn2c1CN1CCOCC1
Reaction #160893
desired product
Rendement 14.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C(=O)Nc2cccc(C(F)(F)F)c2)cc1-c1ccc(N)cc1
Reaction #164893
4′-Amino-6-methyl-N-[3-(trifluoromethyl)phenyl]biphenyl-3-carboxamide
DOI: 10.6084/m9.figshare.5104873.v1
Page 1Suivant