trifluoroacetamide

NCc1cc(F)ccc1[N+](=O)[O-]
Reaction #41762
(5-fluoro-2-nitrophenyl)methylamine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NCC=CCl)C(F)(F)F
Reaction #46067
N-(3-Chloro-allyl)-2,2,2-trifluoro-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
O=C(NCC=CCl)C(F)(F)F
Reaction #46068
N-(3-Chloro-allyl)-2,2,2-trifluoro-acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2010_06
N=S(=O)(c1ccc([N+](=O)[O-])cc1)C1CC1
Reaction #66480
(RS)—S-(4-nitrophenyl)-S-cyclopropylsulfoximide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_09
O=C(NCc1ccccc1)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)C(F)(F)F
Reaction #216020
(R)-N-(phenylmethyl)-α-[(trifluoroacetyl)amino]-1H-indole-3-propanamide
Yield 66.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1995_11
COc1cccc(CC(O)C2CCNCC2)c1OC
Reaction #222862
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
NC(=O)C(F)(F)F
Reaction #223635
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
CC1COCCN1c1cc(C(C)(C)S(C)(=O)=NC(=O)C(F)(F)F)nc(Cl)n1
Reaction #272672
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
COC(=O)CS(=O)(CC(=O)OC)=NC(=O)C(F)(F)F
Reaction #284119
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(NCCOCCOCCO)C(F)(F)F
Reaction #297284
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1ccc(C(=O)c2cn(Cc3cccc(N)n3)c3ccccc3c2=O)nc1C
Reaction #314297
1-(6-Amino-pyridin-2-ylmethyl)-3-(5,6-dimethyl-pyridine-2-carbonyl)-1H-quinolin-4-one
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
CCNC(=O)Nc1cn2ccc(-c3nc(C)n(C)n3)cc2n1
Reaction #316550
pyrimidine
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2009_07
N=S(=O)(c1ccc([N+](=O)[O-])cc1)C1CC1
Reaction #325315
(RS)—S-(4-nitrophenyl)-S-cyclopropylsulfoximide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_02
O=C1CN(Cc2ccccc2)CC(=O)N1
Reaction #358803
4-benzyl-piperazine-2,6-dione
Yield 73.1%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
O=C1CN(c2ccc(F)cc2)CC(=O)N1
Reaction #358806
4-(4-fluoro-phenyl)-piperazine-2,6-dione
Yield 38.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2008_11
COC(=O)c1cccc(S(C)(=N)=O)c1
Reaction #390710
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CC1(C)Oc2ccc([N+](=O)[O-])cc2C=C1CNC(=O)C(F)(F)F
Reaction #403676
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
O=C(NCCCCc1cccc(O)c1)C(F)(F)F
Reaction #428817
2,2,2-trifluoro-N-(4-(3-hydroxyphenyl)butyl)acetamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2014_11
COC(=O)CCc1ccc(S(C)(=O)=NC(=O)C(F)(F)F)cc1
Reaction #478763
title compound
Yield 69.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
COC(=O)c1cccc(S(C)(=N)=O)c1
Reaction #478779
title compound
Yield 74.2%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2013_02
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