Hydrochloride methanol → HCID 21979793, 화합물
반응식
C(OC([NH:8][CH2:9][CH2:10][CH2:11][N:12]([S:20]([C:23]1[CH:32]=[CH:31][CH:30]=[C:29]2[C:24]=1[CH:25]=[CH:26][N:27]=[CH:28]2)(=[O:22])=[O:21])[CH2:13][CH2:14][C:15]1[S:16][CH:17]=[CH:18][CH:19]=1)=O)(C)(C)C.[ClH:33].CO>>[ClH:33].[CH:28]1[C:29]2[C:24](=[C:23]([S:20]([N:12]([CH2:13][CH2:14][C:15]3[S:16][CH:17]=[CH:18][CH:19]=3)[CH2:11][CH2:10][CH2:9][NH2:8])(=[O:22])=[O:21])[CH:32]=[CH:31][CH:30]=2)[CH:25]=[CH:26][N:27]=1참가 물질
3
실험 절차
According to the method of Example 1, Step C, deprotection was performed (50° C., 2 hours) by using Intermediate 3 (238 mg) and 10% hydrogen chloride/methanol solution (5 ml). The reaction mixture was cooled to room temperature, and then the solvent was evaporated under reduced pressure. The residue was added with methanol (1 ml) and diethyl ether (3 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (202 mg) as white powdery solid.
후처리
- custom(50° C., 2 hours)
- customthe solvent was evaporated under reduced pressure
- additionThe residue was added with methanol (1 ml) and diethyl ether (3 ml)
- customThe deposited precipitates
- filtration