Methyl iodide → HCID 59850229, compound
Reaction equation
[CH2:1]([O:8][C:9]([N:11]([C@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:14]1)[CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(OC(N[C@@H]1CCN(C(OC(C)(C)C)=O)C1)=O)C1C=CC=CC=1.IC>>[CH2:1]([O:8][C:9]([N:11]([C@@H:13]1[CH2:17][CH2:16][N:15]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:14]1)[CH3:12])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 130, starting from tert-butyl (R)-3-benzyloxycarbonylaminopyrrolidine-1-carboxylate (prepared according to Zhou et al, US 2008 0293771) and iodomethane, as a pale coloured oil.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-1665c0cc61354a109689706670934011
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09290472B2
Reaction notes
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