반응식
[Cl:1][C:2]1[N:7]=[C:6]([CH:8]=C)[C:5]([O:10][CH3:11])=[C:4]([Cl:12])[N:3]=1.C[OH:14].ClCCl>>[Cl:1][C:2]1[N:7]=[C:6]([CH:8]=[O:14])[C:5]([O:10][CH3:11])=[C:4]([Cl:12])[N:3]=1참가 물질
3
실험 절차
A solution of 2,6-dichloro-5-methoxy-4-vinyl pyrimidine (6.64 g, 32.5 mmol, prepared by Example 2), in methanol:dichloromethane (1:4, 300 mL), was cooled to −78° C. in a dry ice/acetone bath. Ozone was bubbled into the reaction until the starting material was no longer present according to thin layer chromatography (TLC). Dimethyl sulfide (6 mL) was added. The mixture was concentrated on a rotary evaporator at 0° C. to remove the dichloromethane. This provided an unpurified material comprising the title compound. The title compound was not isolated from the unpurified material.
후처리
- customOzone was bubbled into the reaction until the starting material
- additionDimethyl sulfide (6 mL) was added
- concentrationThe mixture was concentrated on a rotary evaporator at 0° C.
- customto remove the dichloromethane
- customThis provided an unpurified material
출처 및 근거
- ORD 기록
- ord-f1c2a354e193464487024d532308cd16
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08877925B2
연결된 노트
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