2-(Pyrrolidin-3-yl)pyridine → 2(S)-hydroxy-3(R)-[3(R/S)-pyridin-2-yl-pyrrolidine-1-carbonyl)-heptanoic acid
Reaction equation
CC1(C)[O:6][C:5](=[O:7])[CH:4]([CH:8]([CH2:12][CH2:13][CH2:14][CH3:15])[C:9]([OH:11])=O)[O:3]1.[NH:17]1[CH2:21][CH2:20][CH:19]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=2)[CH2:18]1>>[OH:3][C@@H:4]([C@H:8]([C:9]([N:17]1[CH2:21][CH2:20][CH:19]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=2)[CH2:18]1)=[O:11])[CH2:12][CH2:13][CH2:14][CH3:15])[C:5]([OH:6])=[O:7]Participants
3
Procedure
The title compound is prepared from 2-(2,2-dimethyl-4-oxo-1,3-dioxolan-5-yl)hexanoic acid B-5 and commercially available 2-pyrrolidin-3-yl-pyridine A-5 according to General Procedure B.
Sources & evidence
- ORD record
- ord-b5aeb1364c414142b2de1e16b42226e1
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612059B2
Reaction notes
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