반응식
[S:1]1[CH:5]=[C:4]([CH2:6][OH:7])[N:3]=[N:2]1.C(N(CC)CC)C.[CH3:15][S:16](Cl)(=[O:18])=[O:17]>ClCCl>[CH3:15][S:16]([O:7][CH2:6][C:4]1[N:3]=[N:2][S:1][CH:5]=1)(=[O:18])=[O:17]참가 물질
5
실험 절차
A solution of 1,2,3-thiadiazol-4-ylmethanol (0.75 g, 6.5 mmol) in dichloromethane (20 mL) was cooled to 5° C. under a nitrogen atmosphere and treated with triethylamine (1.018 mL, 7.3 mmol) and methanesulfonyl chloride (0.565 mL, 7.3 mmol). After 15 min, the ice-bath was removed and the reaction mixture was stirred for 2 h. The solution was washed with 1N hydrochloric acid solution (2×2 mL) and water, dried (MgSO4 +MgO) and concentrated. The residue was purified by chromatography (silica gel column 1.5×21 cm) with ether as eluting solvent to give 0.90 g (71%) of 1,2,3-thiadiazol-4-ylmethanol methanesulfonate;
후처리
- customthe ice-bath was removed
- washThe solution was washed with 1N hydrochloric acid solution (2×2 mL) and water
- dry with materialdried (MgSO4 +MgO)
- concentrationconcentrated
- customThe residue was purified by chromatography (silica gel column 1.5×21 cm) with ether
- washas eluting solvent
출처 및 근거
- ORD 기록
- ord-0e077cfc447e42b8a18740511d4ae4da
- 출처 데이터셋
- uspto-grants-1988_05
- 특허 번호
- US04746736
연결된 노트
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