Nitric Acid → 6-methyl-5-nitro-3-propyl-1,3-dihydropyrimidine-2,4-dione
반응식
[CH2:1]([N:4]1[C:9](=[O:10])[CH:8]=[C:7]([CH3:11])[NH:6][C:5]1=[O:12])[CH2:2][CH3:3].OS(O)(=O)=O.[N+:18]([O-])([OH:20])=[O:19]>O>[CH3:11][C:7]1[NH:6][C:5](=[O:12])[N:4]([CH2:1][CH2:2][CH3:3])[C:9](=[O:10])[C:8]=1[N+:18]([O-:20])=[O:19]참가 물질
5
실험 절차
3-propyl-6-methyl-1,3-dihydropyrimidine-2,4-dione (3 g), as prepared in Example 3, was added to a solution of concentrated H2SO4 (12 ml) and HNO3 (9.6 ml) at 0° C. The reaction mixture was allowed to come to room temperature and continued stirring for another 2 h. The reaction mixture was then poured into water and extracted with ethyl acetate (3×50 mL). The organic layer was washed with water, brine and dried over Na2SO4. Removal of the solvent and recrystallization of the residue with ethylacetate/hexane mixture furnished the 6-methyl-5-nitro-3-propyl-1,3-dihydropyrimidine-2,4-dione(1.56 g).
후처리
- customto come to room temperature
- extractionextracted with ethyl acetate (3×50 mL)
- washThe organic layer was washed with water, brine
- dry with materialdried over Na2SO4
- customRemoval of the solvent and recrystallization of the residue with ethylacetate/hexane mixture
출처 및 근거
- ORD 기록
- ord-36a7fa056d7a45c28b40a06e951abd6c
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07449473B2
반응 노트
불러오는 중…