돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 245304생성일: 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/245304

반응식

참여 물질

역할이름HCID투입량
반응물Butyl iodideHCID 10962—
반응물Lithium CarbonateHCID 11125—
반응물4-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-ethenylpyrimidine-6-carboxylic acidHCID 46850912—
용매DimethylformamideHCID 6228—
생성물6-Amino-2-(4-chloro-2-fluoro-3-methoxyphenyl)-5-vinyl-pyrimidine-4-carboxylic acid butyl esterHCID 5943208752.7%

반응 조건

온도60 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08658791B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-f1786629b665455cb6b49adf475e259f
출처 메모uspto-grants-2014_02