반응식
[CH:1]1([CH2:4][OH:5])[CH2:3][CH2:2]1.[H-].[Na+].Cl[C:9]1[C:10]([C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[N:11][S:12][N:13]=1.O>O1CCCC1>[CH:1]1([CH2:4][O:5][C:9]2[C:10]([C:14]3[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=3)=[N:11][S:12][N:13]=2)[CH2:3][CH2:2]1참가 물질
6
실험 절차
To a solution of cyclopropylcarbinol (360 mg, 5 mmol) and sodium hydride (110 m, 5 mmol) in dry tetrahydrofuran was added a solution of 3-(4-chloro-1,2,5-thiadiazol-3-yl)pyridine (490 mg, 2.5 mmol) in dry tetrahydrofuran. The reaction mixture was stirred at room temperature for 3 h. Water was added and the mixture was extracted with ether. The ether phase was dried and evaporated to yield 400 m (69%) of the title compound.
후처리
- extractionthe mixture was extracted with ether
- dry with materialThe ether phase was dried
- customevaporated
출처 및 근거
- ORD 기록
- ord-3cf78650f1584145a9c7d7aef6731b11
- 출처 데이터셋
- uspto-grants-1998_01
- 특허 번호
- US05712297
연결된 노트
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