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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432846생성일: 2026년 10월 25일

Heptanoyl chloride → N-(4-[{5-(methylthio)pentyl]amino}quinolin-3-yl)heptanamide

https://huagongshe.com/reaction/432846

반응식

참여 물질

역할이름HCID투입량
반응물Heptanoyl chlorideHCID 17313—
반응물N4-[5-(methylthio)pentyl]quinoline-3,4-diamineHCID 22320477—
용매PyridineHCID 1049—
생성물N-(4-[{5-(methylthio)pentyl]amino}quinolin-3-yl)heptanamideHCID 22320422100%

반응 조건

온도0 °C

반응 단계

A round bottom flask was charged with a magnetic stir bar, N4-[5-(methylthio)pentyl]quinoline-3,4-diamine (3.17 g, 11.46 mmol) and anhydrous pyridine (46 mL) under a nitrogen atmosphere. The resulting homogeneous solution was cooled to 0° C. in an ice-water bath. To the cooled solution was added neat heptanoyl chloride (1.87 g, 12.61 mmol). The reaction was judged to be complete after stirring at ambient temperature for 1 hour. The volatiles were removed under reduced pressure and the resulting oil was partitioned between chloroform and water. The layers were separated. The organic layer was washed with saturated aqueous sodium bicarbonate and brine, dried over anhydrous sodium sulfate, filtered and then concentrated under reduced pressure to afford N-(4-{[5-(methylthio)pentyl]amino}quinolin-3-yl)heptanamide (4.44 g, 11.46 mmol) which was isolated as a brown oil and used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664264B2
출처 데이터셋uspto-grants-2003_12
ORD IDord-4701c5247d6640a1bc8c38ec08eaacb9
출처 메모uspto-grants-2003_12