Thionyl Chloride → 2-Chloromethyl-imidazo(1,2-A)pyridine
반응식
O[CH2:2][C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[CH:11]=1.S(Cl)([Cl:14])=O>C(Cl)Cl>[Cl:14][CH2:2][C:3]1[N:4]=[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][N:6]2[CH:11]=1참가 물질
4
실험 절차
In a round bottomed flask containing 2-hydroxymethyl-imidazo[1,2-a]pyridine (800 mg, 5.4 mmol) in DCM (8 mL), was added at R.T. thionyl chloride (1.96 mL, 27 mmol). The solution became clear and 10 min later, a precipitated was formed. The reaction mixture was stirred at R.T. for 2 hours and the solvent was removed under reduced pressure to afford 1.10 g of a brownish solid as the chlorhydrate form of 2-(chloromethyl)-imidazo[1,2-a]pyridine (Yield: 100%).
후처리
- customlater, a precipitated was formed
- customthe solvent was removed under reduced pressure
출처 및 근거
- ORD 기록
- ord-5f0681e12ce54d23b716f98f63a84336
- 출처 데이터셋
- uspto-grants-2012_01
- 특허 번호
- US08101637B2
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