Thionyl Chloride → 3-(Chloromethyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine hydrochloride
반응식
[N:1]1[CH:2]=[C:3]([CH2:10]O)[N:4]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=12.S(Cl)([Cl:14])=O>>[ClH:14].[Cl:14][CH2:10][C:3]1[N:4]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]2=[N:1][CH:2]=1참가 물질
3
실험 절차
To 5,6,7,8-tetrahydroimidazo[1,2-a]pyridin-3-yl methanol (1.0 g), thionyl chloride (5 ml) was added at 0° C. After heating to reflux for 40 minutes, the mixture was concentrated under reduced pressure. To the residue was added ethyl acetate, and the precipitated crystals were collected by filtration. The crystals were washed with ethyl acetate, to give 3-(chloromethyl)-5,6,7,8-tetrahydroimidazo[1,2-a]pyridine hydrochloride (1.03 g) as pale yellow crystals.
후처리
- temperatureAfter heating
- temperatureto reflux for 40 minutes
- concentrationthe mixture was concentrated under reduced pressure
- additionTo the residue was added ethyl acetate
- filtrationthe precipitated crystals were collected by filtration
- washThe crystals were washed with ethyl acetate
출처 및 근거
- ORD 기록
- ord-5a113966d87b4507ad2682dc12a781c3
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07262185B2
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