Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2386152생성일: 2026년 10월 25일
Butyl iodide → 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid butyl ester
https://huagongshe.com/reaction/2386152
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Butyl iodide | HCID 10962 | — |
| 반응물 | Lithium Carbonate | HCID 11125 | — |
| 반응물 | 4-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-ethenylpyrimidine-6-carboxylic acid | HCID 46850912 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid butyl ester | HCID 59432087 | 52.7% |
반응 단계
6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid (0.150 g, 0.46 mmol), iodobutane (0.111 g, 0.60 mmol), and lithium carbonate (0.044 g, 0.6 mmol) were combined in DMF (1.5 mL) and heated at 60° C. overnight. The cooled reaction mixture was concentrated and partitioned between ethyl acetate and water. The organic phase was dried and concentrated. The product was purified by flash chromatography on silica gel (ethyl acetate/hexane gradient) to yield the title compound (0.092 g, 52.3% yield): 1H NMR (CDCl3) δ 7.65 (dd, 1H), 7.19 (dd, 1H), 7.75 (dd, 1H), 5.62-5.67 (m, 2H), 5.35 (br s, 2H), 4.34 (t, 3H), 3.99 (dd, 3H), 1.74 (m, 2H), 1.45 (m, 2H), 0.97 (t, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08268753B2 |
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| 출처 데이터셋 | uspto-grants-2012_09 |
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| ORD ID | ord-9ce36516649743049d0f86678bfd9242 |
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| 출처 메모 | uspto-grants-2012_09 |
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