Triethylamine → 1,2,3-Thiadiazol-4-ylmethanol methanesulfonate

HRID 569668

반응식

HRID 569668 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

  1. customthe ice-bath was removed
  2. washThe solution was washed with 1N hydrochloric acid solution (2×2 mL) and water
  3. dry with materialdried (MgSO4 +MgO)
  4. concentrationconcentrated
  5. customThe residue was purified by chromatography (silica gel column 1.5×21 cm) with ether
  6. washas eluting solvent

출처 및 근거

ORD 기록
ord-8499bae8663146e9bbdf2abc9c1fe95f
출처 데이터셋
uspto-grants-1988_03
특허 번호
US04732977

연결된 노트

불러오는 중…