An 325 Reaktionen beteiligt

18200

O=C(Nc1cc(Br)cnc1O)c1ccc(C(F)(F)F)cc1
Reaction #7901
title compound
Ausbeute 60.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=C1CCC(N2C(=O)c3cccc(NC(=O)c4ccc(C(F)(F)F)cc4)c3C2=O)C(=O)N1
Reaction #10104
N-[2-(2,6-dioxo-piperidin-3-yl)-1,3-dioxo-2,3-dihydro-1H-isoindol-4-yl]-4-trifluoromethyl-benzamide
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
COc1cc(Nc2cncc(-c3ccc(C(=O)c4ccc(C(F)(F)F)cc4)cc3N)n2)cc(OC)c1OC
Reaction #44594
title compound
Ausbeute 46.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
—
Reaction #54529
colorless needles
Ausbeute 77.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1979_04
—
Reaction #56968
solid
Ausbeute 63.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
CC(C)(C)OC(=O)c1ccc(OCCO/N=C/c2ccc(C(C)(C)C)cc2)cc1OC(=O)c1ccc(C(F)(F)F)cc1
Reaction #57928
4-{2-[({(E)-[4-(tert-butyl)phenyl]methylidene}amino)oxy]ethoxy}-2-{[4-(trifluoromethyl)benzoyl]oxy}benzoic acid tert-butyl ester
Ausbeute 96.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=[N+]([O-])c1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3)n2)nc1
Reaction #60153
{5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}{2-[(5-nitro(2-pyridyl))amino]ethyl}amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
N#Cc1ccc(NCCNc2ncc(-c3ncc[nH]3)c(-c3ccc(C(F)(F)F)cc3)n2)nc1
Reaction #60154
6-{[2-({5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}amino)ethyl]-amino}pyridine-3-carbonitrile
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
FC(F)(F)c1ccc(-c2nc(NCCNc3ccc(C(F)(F)F)cn3)ncc2-c2ncc[nH]2)cc1
Reaction #60155
{5-imidazol-2-yl-4-[4-(trifluoromethyl)phenyl]pyrimidin-2-yl}(2-{[5-(trifluoromethyl)(2-pyridyl)]amino}ethyl)amine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
O=c1nncc2c3c(cccc13)N=C2c1ccc(C(F)(F)F)cc1
Reaction #61625
4-trifluoromethylphenyl-[1,2]diazepino[4,5,6-cd]indol-6-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_09
Cc1nc(NC(=O)c2ccc(C(F)(F)F)cc2)sc1C(=O)NCc1ccccc1
Reaction #73620
title compound
Ausbeute 45.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
C[Si](C)(C)CCOCn1cc(-c2ccncc2)c(-c2cccc(CNC(=O)c3ccc(C(F)(F)F)cc3)c2)n1
Reaction #74108
N-{3-[4-pyridin-4-yl-1-(2-trimethylsilanyl-ethoxymethyl)-1H-pyrazol-3-yl]-benzyl}-4-trifluoromethyl-benzamide
Ausbeute 76.9%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C1CCC(N2Cc3cc(CNC(=O)c4ccc(C(F)(F)F)cc4)ccc3C2=O)C(=O)N1
Reaction #91701
N-[2-(2,6-dioxo-piperidin-3-yl)-1-oxo-2,3-dihydro-1H-isoindol-5-ylmethyl]-4-trifluoromethyl-benzamide
Ausbeute 49.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2016_09
CN(C)C1(CNC(=O)c2ccc(C(F)(F)F)cc2)CCC2(CC1)OCCO2
Reaction #95966
α,α,α-trifluoro-N-[[8-(dimethylamino)-1,4-dioxaspiro[4.5]dec-8-yl]methyl]-p-toluamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1982_08
CCOC(=NC(=O)c1ccc(C(F)(F)F)cc1)N1Cc2ccccc2-c2ccccc2C1
Reaction #177864
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCC(OC(=O)c2ccc(C(F)(F)F)cc2)N(c2nnc(C3CC3)s2)C1=O
Reaction #179991
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C#N)(Cn1cc2ncc(Br)cc2n1)NC(=O)c1ccc(C(F)(F)F)cc1
Reaction #182383
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CC(C)(C)OC(=O)NCC#CC(=O)c1ccc(C(F)(F)F)cc1
Reaction #183725
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
CN1CCN(c2cccc3c2CC(NC(=O)c2ccc(C(F)(F)F)cc2)CC3)CC1
Reaction #190115
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
O=Cc1ccc(C(F)(F)F)cc1
Reaction #193840
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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