Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chloride → 6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chloride | HCID 312 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Butanol, 4-bromo-, 1-acetate | HCID 78491 | — |
| 반응물 | 6-Amino-2-methoxy-3,4-dihydropyrimidin-4-one | HCID 135404214 | — |
| 용매 | Acetone | HCID 180 | — |
| 생성물 | 6-Amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine | HCID 23499088 | 42% |
반응 단계
Alternative Method B. A mixture of 6-amino-2-methoxy-4-pyrimidone (30 g, 212.6 mmol), K2CO3 (44 g, 318 mmol), benzyltriethylammionium chloride (20 g, 88 mmol) and 4-bromobutyl acetate (60 g, 308 mmol) in acetone (800 ml) was heated at reflux overnight. After cooling to room temperature, the insoluble salts were filtered off and the solvent was removed. The residue was purified by chromatography on silica gel with CHCl3/MeOH (100:2-100:5) as eluent. After separation of 6-amino-2-methoxy-4-(4-acetoxybutyl)pyrimidine (22.8, yield 42%), 18.7 g (yield 34.5%) of 6-amino-2-methoxy-3-(4-acetoxybutyl)-4-pyrimidone was isolated as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06777420B2 |
| 출처 데이터셋 | uspto-grants-2004_08 |
| ORD ID | ord-c02c628edb0048c4a13daa4ec2f86a16 |
| 출처 메모 | uspto-grants-2004_08 |