2,2,2-trifluoroethanesulfonyl chloride

NS(=O)(=O)CC(F)(F)F
Reaction #9349
CF3CH2SO2NH2
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2006_08
O=S(=O)(CC(F)(F)F)NCC1CC1(c1ccccc1)c1ccc2c(cnn2-c2ccc(F)cc2)c1
Reaction #175526
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
N#Cc1ccc(-c2cccc(N(Cc3cccnc3)S(=O)(=O)CC(F)(F)F)c2)cc1
Reaction #200286
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
C[Si](C)(C)CCOCn1ccc2nc(NC(=O)NC3CCCN(S(=O)(=O)CC(F)(F)F)C3)cnc21
Reaction #210081
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Cl
Reaction #213659
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
NC(=O)c1cc(-c2ccccc2)cc2c(C3CCN(S(=O)(=O)CC(F)(F)F)CC3)n[nH]c12
Reaction #247366
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Cn1c(-c2cncc(CNS(=O)(=O)CC(F)(F)F)c2)cc2ccccc21
Reaction #262043
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=S(=O)(CC(F)(F)F)NCCc1nccn1CCCCc1ccc(OCc2coc(C=Cc3ccc(C(F)(F)F)cc3)n2)cc1
Reaction #266779
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
O=C(Nc1nccs1)C(CC1CCCC1)c1ccc(NS(=O)(=O)CC(F)(F)F)cc1
Reaction #274455
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cc1nc2cccc3n(CCCCCNS(=O)(=O)CC(F)(F)F)c(=O)c1n23
Reaction #285771
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
N#Cc1ccc(-c2cncc(NS(=O)(=O)CC(F)(F)F)c2)cc1Cl
Reaction #301166
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
Cn1ncc2cc([C@H](c3ccccc3)C(C)(C)CNC(=O)CC(F)(F)F)ccc21
Reaction #305315
(S)—N-(2,2-dimethyl-3-(1-methyl-1H-indazol-5-yl)-3-phenylpropyl)-3,3,3-trifluoropropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
Cn1ncc2cc([C@H](c3ccccc3)C(C)(C)CNC(=O)CC(F)(F)F)ccc21
Reaction #305316
(S)—N-(2,2-dimethyl-3-(1-methyl-1H-indazol-5-yl)-3-phenylpropyl)-3,3,3-trifluoropropanamide
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=S(=O)(CC(F)(F)F)NCC1CC1(c1ccccc1)c1ccc2c(cnn2-c2ccc(F)cc2)c1
Reaction #305320
2,2,2-trifluoro-N-((2-(1-(4-fluorophenyl)-1H-indazol-5-yl)-2-phenylcyclopropyl)methyl)ethanesulfonamide
Ausbeute 86.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
O=C(NCCC(c1ccccc1)c1ccc2c(cnn2-c2ccc(F)cc2)c1)C(F)(F)F
Reaction #305343
2,2,2-trifluoro-N-(3-(1-(4-fluorophenyl)-1H-indazol-5-yl)-3-phenylpropyl)acetamide
Ausbeute 99.7%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2012_06
COC(=O)c1sc(-c2cccc(NS(=O)(=O)CC(F)(F)F)c2)c(Br)c1OCC(=O)OC(C)(C)C
Reaction #404103
DOI: 10.1039/C8SC04228DTraining data from https://doi.org/10.1039/C8SC04228D (8/10)
CCOC(=O)c1cc2cc(CC3(C)OCCO3)ccc2n1Cc1ccc(NS(=O)(=O)CC(F)(F)F)cc1
Reaction #429989
title compound
Ausbeute 105.4%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-1999_01
COc1ccccc1Oc1cccc(N(Cc2cccnc2)S(=O)(=O)CC(F)(F)F)c1
Reaction #479572
title compound
Ausbeute 50.0%DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
COc1ccccc1Oc1ccc(N(Cc2cccnc2)S(=O)(=O)CC(F)(F)F)cc1
Reaction #479583
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
O=S(=O)(CC(F)(F)F)NCc1cnccc1-c1cccc(OCc2ccccc2)c1
Reaction #479584
title compound
DOI: 10.6084/m9.figshare.5104873.v1uspto-grants-2004_10
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