Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Bromopinacolone → 5-Ethoxycarbonyl-2-methyl-3-(2-oxo-3,3-dimethyl-butyl)pyrimid-4-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Bromopinacolone | HCID 21642 | — |
| 반응물 | Ethyl 4-hydroxy-2-methylpyrimidine-5-carboxylate | HCID 293750 | — |
| 반응물 | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | 5-Ethoxycarbonyl-2-methyl-3-(2-oxo-3,3-dimethyl-butyl)pyrimid-4-one | HCID 18619693 | — |
반응 단계
To a suspension of 5-ethoxycarbonyl-2-methylpyrimid-4-one (2.7 g, 14.75 mmol.) in DME (20 ml), tetrabutylammonium fluoride (22 ml, 22.0 mmol.) was added. The solution was stirred at room temperature until solids dissolved, then 1-bromopinacolone (2.2 ml, 1.1 eq., 16.22 mmol) was added. The solution was stirred overnight and concentrated to a brown oil. The crude mixture was purified by silica gel column chromatography (hexane/ethyl acetate, 100/0 to 0/100). A less polar O-alkylated by-product was eluted first (1.8 g) and then the desired N-alkylated product (1.1 g); MS (281, M+H)+. NMR (CDCl3, δ): 8.57 (1H, s) , 5.06(1H, s), 4.35(2H, q), 2.42 (3H, s), 1.34 (3H, t), 1.30 (9H,s).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06537998B1 |
| 출처 데이터셋 | uspto-grants-2003_03 |
| ORD ID | ord-48787509fcbd49089b41334e8d0e00ac |
| 출처 메모 | uspto-grants-2003_03 |