2,2,3,3,3-Pentafluoropropyl trifluoromethanesulfonate → (2S,4R)-1-(2,2,3,3,3-pentafluoro-propyl)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide
Reaction equation
Cl.[C:2]([C:4]1([NH:7][C:8]([C@@H:10]2[CH2:14][C@@H:13]([S:15]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[C:24]([F:27])([F:26])[F:25])(=[O:17])=[O:16])[CH2:12][NH:11]2)=[O:9])[CH2:6][CH2:5]1)#[N:3].[F:28][C:29]([F:43])([C:39]([F:42])([F:41])[F:40])[CH2:30]OS(C(F)(F)F)(=O)=O>>[C:2]([C:4]1([NH:7][C:8]([C@@H:10]2[CH2:14][C@@H:13]([S:15]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=3[C:24]([F:27])([F:25])[F:26])(=[O:17])=[O:16])[CH2:12][N:11]2[CH2:30][C:29]([F:43])([F:28])[C:39]([F:42])([F:41])[F:40])=[O:9])[CH2:5][CH2:6]1)#[N:3]Participants
3
Reactant 2
Product 1
Procedure
(2S,4R)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide hydrochloride from experiment K5 was reductively aminated with 2,2,3,3,3-pentafluoropropyltrifluoromethane sulfonate in analogy to experiment L3 to give (2S,4R)-1-(2,2,3,3,3-pentafluoro-propyl)-4-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidine-2-carboxylic acid (1-cyano-cyclopropyl)-amide as a pale brown oil. MS: 520.1 [M+H]+.
Sources & evidence
- ORD record
- ord-0cd0fca7ad1f4b9488d243c99f97c4c7
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163793B2
Reaction notes
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