(R)-2-methyl-1-((S)-pyrrolidin-2-ylmethyl)pyrrolidine → HCID 11675951, compound
Reaction equation
CO[C:3](=[O:20])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[N:13]=2)=[CH:6][C:5]=1[F:19].[CH3:21][C@@H:22]1[CH2:26][CH2:25][CH2:24][N:23]1[CH2:27][C@@H:28]1[CH2:32][CH2:31][CH2:30][NH:29]1>>[F:19][C:5]1[CH:6]=[C:7]([O:10][CH2:11][C:12]2[CH:17]=[CH:16][CH:15]=[C:14]([CH3:18])[N:13]=2)[CH:8]=[CH:9][C:4]=1[C:3]([N:29]1[CH2:30][CH2:31][CH2:32][C@H:28]1[CH2:27][N:23]1[CH2:24][CH2:25][CH2:26][C@H:22]1[CH3:21])=[O:20]Participants
3
Procedure
The title compound is prepared in a manner substantially analogous to Procedure F from 2-Fluoro-4-(6-methyl-pyridin-2-ylmethoxy)-benzoic acid methyl ester and 2-(R)-Methyl-1-(2-(S)-pyrrolidinylmethyl)pyrrolidine. MS (ES+) 412.3
Sources & evidence
- ORD record
- ord-f8a1e0a2d07c4616a1ef2333bf0af5bc
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696234B2
Reaction notes
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