반응식
[S:1]1[C:9]2[CH:8]=[CH:7][NH:6][C:5](=O)[C:4]=2[CH:3]=[CH:2]1.P(Cl)(Cl)([Cl:13])=O>>[Cl:13][C:5]1[C:4]2[CH:3]=[CH:2][S:1][C:9]=2[CH:8]=[CH:7][N:6]=1참가 물질
3
반응 조건
- 온도
- 100 °C
실험 절차
5H-Thieno[3,2-c]pyridin-4-one (1.0 g, 6.62 mmol) is dissolved in 30 mL of phosphorous oxy chloride. The solution is heated to 100° C. After 4 hours, the solution is concentrated. The residue is dissolved in CH2Cl2. The resulting solution is washed with water and saturated NaCl. The organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with a gradient of 40% CH2Cl2 /hexanes to 60% CH2Cl2 /hexanes. The title compound (1.0 g, 5.8 mmol) is obtained as a white solid.
후처리
- concentrationthe solution is concentrated
- dissolutionThe residue is dissolved in CH2Cl2
- washThe resulting solution is washed with water and saturated NaCl
- dry with materialThe organic layer is dried over MgSO4
- filtrationfiltered
- concentrationconcentrated
- customThe crude product is purified by column chromatography
- washeluting with a gradient of 40% CH2Cl2 /hexanes to 60% CH2Cl2 /hexanes
출처 및 근거
- ORD 기록
- ord-0c279f7fd02d414880916db47fdc6e15
- 출처 데이터셋
- uspto-grants-2000_03
- 특허 번호
- US06034093
연결된 노트
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