Pyrrolidine → HCID 57980139, compound
Reaction equation
O[CH2:2][C@H:3]1[CH2:7][CH2:6][CH2:5][N:4]1[C:8]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=2)=[CH:12][CH:11]=1)=[O:9].[NH:26]1[CH2:30][CH2:29][CH2:28][CH2:27]1>>[N:26]1([CH2:2][C@H:3]2[CH2:7][CH2:6][CH2:5][N:4]2[C:8]([C:10]2[CH:15]=[CH:14][C:13]([C:16]3[CH:21]=[CH:20][C:19]([C:22]([F:25])([F:24])[F:23])=[CH:18][CH:17]=3)=[CH:12][CH:11]=2)=[O:9])[CH2:30][CH2:29][CH2:28][CH2:27]1Participants
3
Procedure
The title compound is prepared in a manner substantially analogous to Procedure RR starting from (2-(R)-hydroxymethyl-pyrrolidin-1-yl)-(4′-trifluoromethyl-biphenyl-4-yl)-methanone and pyrrolidine. MS (M+H) 403.2
Sources & evidence
- ORD record
- ord-3795f5230159423293ef51aa7167cadc
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07632857B2
Reaction notes
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