반응식
[NH2:1][C:2]1[N:7]=[C:6](O)[CH:5]=[C:4]([C:9]([CH3:12])([CH3:11])[CH3:10])[N:3]=1.P(Cl)(Cl)([Cl:15])=O>>[NH2:1][C:2]1[N:7]=[C:6]([Cl:15])[CH:5]=[C:4]([C:9]([CH3:12])([CH3:11])[CH3:10])[N:3]=1참가 물질
3
실험 절차
2-Amino-4-hydroxy-6-tert-butylpyrimidine (8.35 g) was dissolved in 50 mL of phosphorus oxychloride and the solution refluxed for 2 hours. Excess phosphorus oxychloride was removed under vacuum and the residue dissolved in 100 mL of ethanol. The solution was adjusted to pH 8 with ice-cold concentrated ammonium hydroxide, and solvent removed under reduced pressure. The residue was filtered to give a white solid, which was recrystallized from ethanol-water to give 2-amino-4-chloro-6-tert-butylpyrimidine (3.66 g), m.p. 87.7-88.90° C.
후처리
- temperaturethe solution refluxed for 2 hours
- customExcess phosphorus oxychloride was removed under vacuum
- dissolutionthe residue dissolved in 100 mL of ethanol
- customremoved under reduced pressure
- filtrationThe residue was filtered
- customto give a white solid, which
- customwas recrystallized from ethanol-water
출처 및 근거
- ORD 기록
- ord-99e6e0411197410d89d6f00a4595dbde
- 출처 데이터셋
- uspto-grants-1999_09
- 특허 번호
- US05952331
연결된 노트
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