Methyl L-prolinate → HCID 86679124, compound
Reaction equation
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][CH2:8][CH2:7][NH:6]1)=[O:4].[Br:10][C:11]1[CH:12]=[N:13][CH:14]=[C:15]([CH2:17]Cl)[CH:16]=1>>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][CH2:8][CH2:7][N:6]1[CH2:17][C:15]1[CH:14]=[N:13][CH:12]=[C:11]([Br:10])[CH:16]=1)=[O:4]Participants
3
Procedure
In analogy to the procedure described for the preparation of intermediates B-1 [B], (S)-pyrrolidine-2-carboxylic acid methyl ester has been coupled to 3-bromo-5-chloromethyl-pyridine (intermediate B-1 [A]) to yield the title compound as light yellow oil. MS: 299.2, 301.1 (M+H+).
Sources & evidence
- ORD record
- ord-5c62e7c73e304053ae9ef4917c07d31a
- Source dataset
- uspto-grants-2015_09
- Patent number
- US09133158B2
Reaction notes
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