Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476081생성일: 2026년 10월 26일
Ethyl 4-(4-methoxyphenyl)-2,4-dioxobutanoate → Ethyl 1-(1-methylethyl)-6-[4-(methyloxy)phenyl]-1H-pyrazolo[3,4-b]pyridine-4-carboxylate
https://huagongshe.com/reaction/476081
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl 4-(4-methoxyphenyl)-2,4-dioxobutanoate | HCID 287267 | — |
| 반응물 | 1-(propan-2-yl)-1H-pyrazol-5-amine | HCID 1090341 | — |
| 용매 | Benzene | HCID 241 | — |
| 생성물 | Ethyl 1-(1-methylethyl)-6-[4-(methyloxy)phenyl]-1H-pyrazolo[3,4-b]pyridine-4-carboxylate | HCID 67124614 | 65.1% |
반응 단계
To a solution of ethyl 4-[4-(methyloxy)phenyl]-2,4-dioxobutanoate (600 mg, 2.397 mmol) in benzene (5 mL) was added 1-(1-methylethyl)-1H-pyrazol-5-amine (300 mg, 2.397 mmol), and the reaction mixture was stirred at 62° C. overnight. The mixture was concentrated in vacuo and the residue was dissolved into acetic acid (3 mL). The solution was stirred at reflux for 1 h and concentrated in vacuo. The residue was purified using column chromatography (Silica gel, 0 to 100% EtOAc/hexanes) to give 530 mg (65%) of product. LCMS E-S (M+H)=340.1 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.47-1.57 (m, 3H), 1.61-1.71 (m, 6H), 3.88-3.96 (s, 3H), 4.55 (q, J=7.2 Hz, 2H), 5.46 (m, 1H), 7.03-7.12 (m, 2H), 8.13-8.25 (m, 3H), 8.36-8.43 (m, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637509B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-d9ff0b00a30345438d532d0d44edb931 |
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| 출처 메모 | uspto-grants-2014_01 |
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