N-Iodosuccinimide → 5-(4-Ethylphenyl)-6-iodofuro[2,3-d]pyrimidin-4(3H)-one
반응식
[I:1]N1C(=O)CCC1=O.[CH2:9]([C:11]1[CH:16]=[CH:15][C:14]([C:17]2[C:25]3[C:24](=[O:26])[NH:23][CH:22]=[N:21][C:20]=3[O:19][CH:18]=2)=[CH:13][CH:12]=1)[CH3:10]>C(#N)C.ClC(Cl)(Cl)Cl>[CH2:9]([C:11]1[CH:12]=[CH:13][C:14]([C:17]2[C:25]3[C:24](=[O:26])[NH:23][CH:22]=[N:21][C:20]=3[O:19][C:18]=2[I:1])=[CH:15][CH:16]=1)[CH3:10]참가 물질
실험 절차
Add 7.0 g (31.3 mmol) of N-iodosuccinimide to a solution of 5.0 g (20.9 mmol) of 5-(4-ethylphenyl)furo[2,3-d]pyrimidin-4(3H)-one in 250 ml of acetonitrile/tetrachloromethane (1:1). Stir the resulting suspension under reflux for two hours. After cooling to room temperature, concentrate the reaction mixture under reduced pressure. Stir the residue in ethyl acetate and filter. Add water to the filtrate. After removal of the organic phase, extract the aqueous phase repeatedly with ethyl acetate. Concentrate the combined organic phases under reduced pressure. Take up the residue in ethyl acetate and chromatograph it on silica gel (eluent: cyclohexane/ethyl acetate 1:1→1:2). Stir the resulting solid in diethyl ether/n-pentane and filter. 1.4 g (85% purity, 16% of theory) of the target compound are obtained.
후처리
- temperatureunder reflux for two hours
- concentrationconcentrate the reaction mixture under reduced pressure
- stirringStir the residue in ethyl acetate
- filtrationfilter
- customAfter removal of the organic phase
- extractionextract the aqueous phase repeatedly with ethyl acetate
- concentrationConcentrate the combined organic phases under reduced pressure
- stirringStir the resulting solid in diethyl ether/n-pentane
- filtrationfilter
- custom1.4 g (85% purity, 16% of theory) of the target compound are obtained
출처 및 근거
- ORD 기록
- ord-85a78d902a304e239b90b5a591cb5f0a
- 출처 데이터셋
- uspto-grants-2012_12
- 특허 번호
- US08324222B2
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