Hydrochloride methanol → 4-[(4-Methyl-5-isoquinolyl)oxy]piperidine hydrochloride
반응식
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[O:12][CH:13]2[CH2:18][CH2:17][N:16](C(OC(C)(C)C)=O)[CH2:15][CH2:14]2)[CH:5]=[N:4][CH:3]=1.[ClH:26].CO>>[ClH:26].[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][C:10]=2[O:12][CH:13]2[CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)[CH:5]=[N:4][CH:3]=1참가 물질
3
실험 절차
According to the method of Example 1, Step C, deprotection was performed (room temperature, 2 hours) by using Intermediate 128 (604 mg) and 10% hydrogen chloride/methanol solution (20 ml). The solvent was evaporated under reduced pressure, and the residue was added with methanol (5 ml) and diethyl ether (15 ml). The deposited precipitates were collected by filtration and washed with diethyl ether to obtain the title compound (513 mg).
후처리
- custom(room temperature, 2 hours)
- customThe solvent was evaporated under reduced pressure
- additionthe residue was added with methanol (5 ml) and diethyl ether (15 ml)
- customThe deposited precipitates
- filtration