Bromotrimethylsilane → (S)-4-Azido-1-[[hydroxy(4-phenylbutyl)phosphinyl]acetyl]-L-proline, methyl ester
反応式
[N:1]([CH:4]1[CH2:8][N:7]([C:9](=[O:26])[CH2:10][P:11]([O:23]CC)([CH2:13][CH2:14][CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:12])[C@H:6]([C:27]([O:29][CH3:30])=[O:28])[CH2:5]1)=[N+:2]=[N-:3].Br[Si](C)(C)C>ClCCl>[N:1]([CH:4]1[CH2:8][N:7]([C:9](=[O:26])[CH2:10][P:11]([OH:23])([CH2:13][CH2:14][CH2:15][CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:12])[C@H:6]([C:27]([O:29][CH3:30])=[O:28])[CH2:5]1)=[N+:2]=[N-:3]参加物
4
実験手順
(S)-4-Azido-1-[[ethoxy(4-phenylbutyl)phosphinyl]acetyl]-L-proline, methyl ester (1.60 g), dry dichloromethane and bromotrimethylsilane (0.85 g) are stirred under argon at room temperature. After 19 hours, an additional equivalent of bromotrimethylsilane is added and stirring is continued for 2 hours. Excess bromotrimethylsilane and dichloromethane is removed in vacuo and the residue is treated with ethyl acetate/water and stirred for 15 minutes. The layers are separated and the ethyl acetate layer is extracted with saturated sodium bicarbonate. The aqueous extracts are acidified to pH 1.0 with concentrated hydrochloric acid and extracted with ethyl acetate. The extract is washed with water, brine, dried over sodium sulfate, and the solvent stripped to yield 1.35 g of the title compound as an oil.