Methyl iodide → tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate methylsulfonium iodide
反応式
[C:1]([NH:8][C@H:9]([C:14]([NH:16][NH:17][C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[O:15])[CH2:10][CH2:11][S:12][CH3:13])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].C[I:26]>CC(C)=O>[I-:26].[CH3:11][SH2+:12].[C:1]([NH:8][C@H:9]([C:14]([NH:16][NH:17][C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])=[O:15])[CH2:10][CH2:11][S:12][CH3:13])([O:3][C:4]([CH3:6])([CH3:5])[CH3:7])=[O:2]参加物
4
実験手順
A solution of the resultant tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate in acetone (20 ml) was combined with methyl iodide (17 ml, 240 mmol) and stirred at room temperature overnight. The reaction mixture was concentrated, and the resultant residue was triturated from ether, collected by filtration, washed with ether and dried to obtain tert-butyl 2-(Boc-L-methionyl)-1-hydrazine carboxylate methylsulfonium iodide (19.14 g) as a colorless solid.