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HRID 432846作成日:2026年10月26日

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

https://huagongshe.com/reaction/432846

反応式

関与物質

役割名称HCID仕込み量
反応物Heptanoyl chlorideHCID 17313—
反応物N4-[5-(methylthio)pentyl]quinoline-3,4-diamineHCID 22320477—
溶媒PyridineHCID 1049—
生成物N-(4-[{5-(methylthio)pentyl]amino}quinolin-3-yl)heptanamideHCID 22320422100%

反応条件

温度0 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06664264B2
出典データセットuspto-grants-2003_12
ORD IDord-4701c5247d6640a1bc8c38ec08eaacb9
出典メモuspto-grants-2003_12