Bromomethylcyclopropane → HCID 66771826, compound
Reaction equation
[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C@@H:8]([SH:10])[CH2:7][N:6]1[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])=[O:4].[CH:18]1([CH2:21]Br)[CH2:20][CH2:19]1>>[CH3:1][O:2][C:3]([C@@H:5]1[CH2:9][C@@H:8]([S:10][CH2:21][CH:18]2[CH2:20][CH2:19]2)[CH2:7][N:6]1[C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])=[O:4]Participants
3
Procedure
In analogy to the procedure described in example 409b, (2S,4R)-4-mercapto-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (example 409a) was reacted with cyclopropylmethyl bromide (CAS Reg. No. 7051-34-5) to give the title compound as colorless liquid. MS (ESI): m/z=316.2 [M+H]+.
Sources & evidence
- ORD record
- ord-1d47bb6f1130454da652da02569e37f9
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163793B2
Reaction notes
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