Recherche de Sous-structure

772978

COC(=O)C(CC(F)(F)F)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47617
2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4,4,4-trifluoro-butyric acid methyl ester
Rendement 42.1%DOI: 10.6084/m9.figshare.5104873.v1
O=C(O)C(CC(F)(F)F)N1CC(Oc2ccccc2Cl)=CC1=O
Reaction #47618
2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-4,4,4-trifluoro-butyric acid
Rendement 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CCCCCCC(=O)N(C)C1N(C)C(c2ccc(N3CCCCC3)cc2)=NC1(C(F)(F)F)C(F)(F)F.Cl
Reaction #50582
title compound
Rendement 22.4%DOI: 10.6084/m9.figshare.5104873.v1
CCOc1cc(C(F)(F)F)ccc1C1=NC(c2ccc(Cl)cc2)C(c2ccc(Cl)cc2)N1C(=O)N1CCN(CC(O)C(F)(F)F)CC1
Reaction #59801
[4,5-bis-(4-chloro-phenyl)-2-(2-ethoxy-4-trifluoromethyl-phenyl)-4,5-dihydro-imidazol-1-yl]-[4-(2-hydroxy-2-trifluoromethyethyl)-piperazin-1-yl]-methanone
DOI: 10.6084/m9.figshare.5104873.v1
Cc1nsc(NC(=O)C(C)c2ccc(O)c(NC(=O)CC(F)(F)F)c2)c1Cl
Reaction #76439
N-(4-chloro-3-methylisothiazol-5-yl)-2-[4-hydroxy-3-(3,3,3-trifluoropropionamido)phenyl]propionamide
Rendement 73.5%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(N2CC(O)(C(F)(F)F)N=C2c2ccc(Cl)cc2)cc1
Reaction #80573
2-(4-chlorophenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazole
Rendement 62.0%DOI: 10.6084/m9.figshare.5104873.v1
CS(=O)(=O)c1ccc(-n2cc(C(F)(F)F)nc2-c2ccc(Cl)cc2)cc1
Reaction #80574
2-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazole
Rendement 71.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(C2=NC(O)(C(F)(F)F)CN2c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80591
2-(3-chloro-4-methylphenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-4,5-dihydro-1H-imidazole
Rendement 25.0%DOI: 10.6084/m9.figshare.5104873.v1
Cc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80592
2-(3-chloro-4-methylphenyl)-1-[4-(methylsulfonyl)phenyl]-4-(trifluoromethyl)-1H-imidazole
Rendement 95.0%DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(C2=NC(O)(C(F)(F)F)CN2c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80607
2-(3-chloro-4-methoxyphenyl)-4-hydroxy-1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-4,5-dihydro-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1ccc(-c2nc(C(F)(F)F)cn2-c2ccc(S(C)(=O)=O)cc2)cc1Cl
Reaction #80608
2-(3-chloro-4-methoxyphenyl)-1-[4-(methylsulfonyl)phenyl]-4-trifluoromethyl-1H-imidazole
DOI: 10.6084/m9.figshare.5104873.v1
COc1cn(C(CC(F)(F)F)C(=O)O)c(=O)cc1-c1cc(Cl)ccc1C#N
Reaction #85076
2-[4-(5-Chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4,4,4-trifluorobutanoic acid
DOI: 10.6084/m9.figshare.5104873.v1
CCOC(=O)c1ccc(NC(=O)C(CC(F)(F)F)n2cc(OC)c(-c3cc(Cl)ccc3C#N)cc2=O)cc1
Reaction #85077
Ethyl 4-({2-[4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]-4,4,4-trifluorobutanoyl}amino)benzoate
DOI: 10.6084/m9.figshare.5104873.v1
O=C1CN(C(=O)c2ccc(C3=NOC(c4cc(Cl)cc(C(F)(F)F)c4)(C(F)(F)F)C3)cc2CC(F)(F)F)CN1CCC(F)(F)F
Reaction #92146
1-[(4-[5-[3-chloro-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-4,5-dihydro-1,2-oxazol-3-yl]-2-(2,2,2-trifluoroethyl)phenyl)carbonyl]-3-(3,3,3-trifluoropropyl)imidazolidin-4-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(C(F)(F)F)Cn2c(nc(N3CCOCC3)cc2=O)N1CCc1ccc(Cl)cc1
Reaction #159568
(2S)-1-[2-(4-Chlorophenyl)ethyl]-2-methyl-7-(morpholin-4-yl)-2-(trifluoromethyl)-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(C(F)(F)F)Cn2c(nc(N3CCOCC3)cc2=O)N1CCc1cccc(Cl)c1
Reaction #159569
(2S)-1-[2-(3-Chlorophenyl)ethyl]-2-methyl-7-(morpholin-4-yl)-2-(trifluoromethyl)-2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-one
DOI: 10.6084/m9.figshare.5104873.v1
C[C@@]1(c2cccc(NC(=O)c3ccc(Br)cn3)c2)CO[C@@](C)(C(F)(F)F)C(N)=N1.Cl
Reaction #168751
title compound
DOI: 10.6084/m9.figshare.5104873.v1
Cl.NC(=O)C(N)CC(F)(F)F
Reaction #172106
2-amino-4,4,4-trifluorobutanamide hydrochloride
DOI: 10.6084/m9.figshare.5104873.v1
N#Cc1cc(F)c(NC(CC(F)(F)F)C(N)=O)nc1Cl
Reaction #172107
2-(6-chloro-5-cyano-3-fluoropyridin-2-ylamino)-4,4,4-trifluorobutanamide
Rendement 100.1%DOI: 10.6084/m9.figshare.5104873.v1
CCC(N)C1(C(F)(F)F)CCC(Oc2cc3ccnc(OC)c3cc2Cl)CC1
Reaction #183099
DOI: 10.1039/C8SC04228D
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