反応式
[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]参加物
5
実験手順
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;
後処理
- 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
出典と根拠
- ORDレコード
- ord-8499bae8663146e9bbdf2abc9c1fe95f
- 出典データセット
- uspto-grants-1988_03
- 特許番号
- US04732977
関連ノート
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