Methyl iodide → (R)-4-(benzyloxy)-2-(4-decylphenylsulfonamido)-N,N,N-trimethyl-4-oxobutan-1-aminium iodide
Reaction equation
[CH2:1]([C:11]1[CH:16]=[CH:15][C:14]([S:17]([NH:20][C@@H:21]([CH2:33][N:34]([CH3:36])[CH3:35])[CH2:22][C:23]([O:25][CH2:26][C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=2)=[O:24])(=[O:19])=[O:18])=[CH:13][CH:12]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10].[CH3:37][I:38]>>[I-:38].[CH2:26]([O:25][C:23](=[O:24])[CH2:22][C@@H:21]([NH:20][S:17]([C:14]1[CH:15]=[CH:16][C:11]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10])=[CH:12][CH:13]=1)(=[O:19])=[O:18])[CH2:33][N+:34]([CH3:37])([CH3:36])[CH3:35])[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1Participants
3
Procedure
According to the method described in example S75b, (R)-benzyl 3-(4-decylphenylsulfonamido)-4-(dimethylamino)butanoate was reacted with methyl iodide to give the title compound as a white solid (quantitative). MS ESI 531.4 [M+H]+, calcd for [C30H46N2O4S+H]+ 531.3
Sources & evidence
- ORD record
- ord-8c29602ca83343eca4ef9bc854260ef3
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08410150B2
Reaction notes
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