Hydrochloric Acid → 3-(Imidazol-1-yl)-1-[2-(4-phenylbutyl)phenoxy]-2-propanol hydrochloride
반응식
[ClH:1].[N:2]1([CH2:7][CH:8]([OH:27])[CH2:9][O:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][CH2:18][CH2:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH:6]=[CH:5][N:4]=[CH:3]1>O1CCOCC1.C(OCC)(=O)C>[ClH:1].[N:2]1([CH2:7][CH:8]([OH:27])[CH2:9][O:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=2[CH2:17][CH2:18][CH2:19][CH2:20][C:21]2[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=2)[CH:6]=[CH:5][N:4]=[CH:3]1참가 물질
5
실험 절차
1.7 ml of a 4N solution of hydrogen chloride in dioxane were added to a solution of 790 mg of 3-(imidazol-1-yl)-1-[2-(4-phenylbutyl)phenoxy]-2-propanol [prepared as described in step (a) above] in ethyl acetate, and the resulting mixture was allowed to stand at room temperature for 3 hours. The crystals which precipitated were collected by filtration and dried in vacuo, to give 810 mg (yield 92%) of the title compound as colorless crystals, melting at 128°-130° C.
후처리
- customThe crystals which precipitated
- filtrationwere collected by filtration
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-abf38b009ada4d9a92c86e765741910d
- 출처 데이터셋
- uspto-grants-1996_09
- 특허 번호
- US05556864
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