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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1483생성일: 2026년 10월 23일

Ethyl Acetate → N-{4-Chloro-2-fluoro-5-[hexahydro-2,4,6,-trioxo-3-(2-propynyl)-s-triazin-1-yl]phenyl}-1-cyclohexene-1,2-dicarboximide

https://huagongshe.com/ko/reaction/1483

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
반응물1-(5-Amino-2-chloro-4-fluorophenyl)-3-(2-propynyl)-s-triazine-2,4,6-(1H,3H,5H)-trioneHCID 19690738—
용매Acetic AcidHCID 176—
생성물N-{4-Chloro-2-fluoro-5-[hexahydro-2,4,6,-trioxo-3-(2-propynyl)-s-triazin-1-yl]phenyl}-1-cyclohexene-1,2-dicarboximideHCID 13171989755.9%

반응 단계

A solution of 1-(5-amino-2-chloro-4-fluorophenyl)-3-(2-propynyl)-s-triazine-2,4,6-(1H,3H,5H)-trione (1.50 g, 4.83 mmol), and 3,4,5,6-tetrahydrophthalic anhydride (0.73 g, 4.83 mmol) in acetic acid (3 mL) is heated at 100° C. for 5 hours, cooled, and poured into ethyl acetate, The organic mixture is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate, and concentrated in vacuo to obtain a yellow semi-solid. Flash column chromatography of the semi-solid using silica gel and an ethyl acetate/hexanes (1:2) solution gives the title product as a white solid (1.20 g, mp 127°-135° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726126
출처 데이터셋uspto-grants-1998_03
ORD IDord-9fc8235e42584d779056ec0da7bbdc76
출처 메모uspto-grants-1998_03