Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1662025생성일: 2026년 10월 25일
Ammonium Chloride → Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate
https://huagongshe.com/reaction/1662025
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 반응물 | Ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoate | HCID 66767015 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Ethyl 1-(4-fluorophenyl)-4-methyl-2-oxo-1,2-dihydropyridine-3-carboxylate | HCID 66767143 | 62.5% |
반응 단계
A mixture of ethyl 2-(4-fluorophenylcarbamoyl)-3-methylbut-2-enoate (1.85 g, 6.97 mmol) and N,N-dimethylformamide dimethyl acetal (5 mL, 37.45 mmol) is stirred at 90° C. for 90 min. After the reaction is cooled, EtOAc (30 mL) and saturated NH4Cl solution (20 mL) are added. The organic phase is separated, dried and concentrated. The residue is purified by silica gel column chromatography eluting with DCM:MeOH (10:1). The fractions containing product are concentrated, and the residue is mixed with ether to give 1.2 g of yellow solid which is filtered and discarded. The filtrate is concentrated and purified again by silica gel column chromatography eluting with DCM:MeOH (20:1) to give the product (500 mg, 26% yield). MS (m/z): 276.1 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08030302B2 |
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| 출처 데이터셋 | uspto-grants-2011_10 |
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| ORD ID | ord-b4bec93afae042889ba97f088d11eea0 |
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| 출처 메모 | uspto-grants-2011_10 |
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