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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2269618생성일: 2026년 10월 26일

4-Methylmorpholine → N,N-dihexyl-1,2-dihydro-2-oxoquinoline-3-carboxamide

https://huagongshe.com/reaction/2269618

반응식

참여 물질

역할이름HCID투입량
반응물4-MethylmorpholineHCID 7972—
반응물DihexylamineHCID 8920—
반응물Isobutyl chloroformateHCID 62365—
반응물2-Quinolone-3-carboxylic acidHCID 332488—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물N,N-dihexyl-1,2-dihydro-2-oxoquinoline-3-carboxamideHCID 1546177575.8%

반응 조건

온도-15 °C

반응 단계

In a mixture of 50 ml of tetrahydrofuran and 250 ml of N,N-dimethylformamide were dissolved 9.46 g of 1,2-dihydro-2-oxoquinoline-3-carboxylic acid and 5.06 g of N-methylmorpholine, and after cooling to −15° C., 6.83 g of isobutyl chlorocarbonate was added dropwise over 10 minutes. After stirring at −15° C. for 10 minutes, 9.73 g of dihexylamine was added dropwise over 5 minutes. After stirring at −15° C. for 4 hours and then at room temperature overnight, the reaction mixture was concentrated under reduced pressure, and the residue, after addition of ethyl acetate, was washed with water, 1N hydrochloric acid, a saturated aqueous sodium bicarbonate solution and a saturated aqueous sodium chloride solution, and dried over anhydrous sodium sulfate. After removal of the drying agent by filtration, the filtrate was concentrated under reduced pressure. The residue was recrystallized from hexane to give 13.51 g of N,N-dihexyl-1,2-dihydro-2-oxoquinoline-3-carboxamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06329525B1
출처 데이터셋uspto-grants-2001_12
ORD IDord-29bf628c2e574a03b0bbbdf8a4b778be
출처 메모uspto-grants-2001_12