Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Pyridine → Ethyl 4-(4-fluorophenyl)-3-oxobutanoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | 2,2-Dimethyl-1,3-dioxane-4,6-dione | HCID 16249 | — |
| 반응물 | 4-Fluorophenylacetyl chloride | HCID 3744988 | — |
| 반응물 | 5-(4-Fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid | HCID 60204207 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | Ethyl 4-(4-fluorophenyl)-3-oxobutanoate | HCID 10585213 | — |
반응 단계
The intermediate, 5-(4-fluorophenyl)-4-oxo-1,4-dihydropyridine-3-carboxylic acid (8) can be obtained using the chemistry described in Scheme 2. Thus, 2-(4-fluorophenyl)acetyl chloride (10) can be treated with 2,2-dimethyl-1,3-dioxane-4,6-dione (Meldrum's acid) in the presence of pyridine and the resulting adduct can be refluxed in ethanol to afford ethyl 4-(4-fluorophenyl)-3-oxobutanoate (12). Treatment of intermediate 12 with triazine and sodium ethoxide in ethanol can furnish the requisite ester intermediate, which can be readily hydrolyzed in the presence of sodium hydroxide at elevated temperature to furnish intermediate 8.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08124768B2 |
| 출처 데이터셋 | uspto-grants-2012_02 |
| ORD ID | ord-0d5cdb20972546f3bf686e133ee32594 |
| 출처 메모 | uspto-grants-2012_02 |