4-Fluorobenzoyl chloride → 1-(4-Fluoro-benzoyl)-pyrrolidine-3-carboxylic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4]([CH:6]1[CH2:10][CH2:9][NH:8][CH2:7]1)=[O:5])[CH3:2].[F:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](Cl)=[O:17])=[CH:14][CH:13]=1>>[CH2:1]([O:3][C:4]([CH:6]1[CH2:10][CH2:9][N:8]([C:16](=[O:17])[C:15]2[CH:19]=[CH:20][C:12]([F:11])=[CH:13][CH:14]=2)[CH2:7]1)=[O:5])[CH3:2]Participants
3
Procedure
The title compound was prepared according to the method described for Preparation 2 using pyrrolidine-3-carboxylic acid ethyl ester (see Preparation 1) and 4-fluoro-benzoyl chloride to afford the title compound as a colourless oil (4.3 g, 76%).
Workup
- customThe title compound was prepared
Sources & evidence
- ORD record
- ord-9b6598db7363478d85e9bd0569732f71
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08278343B2
Reaction notes
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