반응식
[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][O:12][CH2:13][CH2:14][N:15]3[CH2:18][CH:17]([OH:19])[CH2:16]3)=[CH:9][C:4]=2[CH:3]=[CH:2]1.[ClH:20]>C(OCC)(=O)C>[ClH:20].[S:1]1[C:5]2[CH:6]=[CH:7][C:8]([CH2:10][CH2:11][O:12][CH2:13][CH2:14][N:15]3[CH2:18][CH:17]([OH:19])[CH2:16]3)=[CH:9][C:4]=2[CH:3]=[CH:2]1참가 물질
4
실험 절차
1.03 g of 1-(2-(2-(1-benzothiophene-5-yl)ethoxy)ethyl)-3-azetidinol was dissolved in 4.2 ml of ethyl acetate. Thereafter, 0.86 ml of an ethyl acetate solution containing 4.76 mol/l dry hydrogen chloride was added to the obtained solution, and the obtained mixture was stirred at a room temperature for 1 hour, and then at 5° C. for 1 hour. Thereafter, precipitated crystals were collected by filtration, washed with ethyl acetate, and then dried, so as to obtain 0.98 g of 1-(2-(2-(1-benzothiophene-5-yl)ethoxy)ethyl)-3-azetidinol hydrochloride.
후처리
- additionwas added to the obtained solution
- waitat 5° C. for 1 hour
- customThereafter, precipitated crystals
- filtrationwere collected by filtration
- washwashed with ethyl acetate
- customdried
출처 및 근거
- ORD 기록
- ord-3374cb4c4ade42af9da5c99d4b443c42
- 출처 데이터셋
- uspto-grants-2011_03
- 특허 번호
- US07897594B2
연결된 노트
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