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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469252생성일: 2026년 10월 26일

Dimethyl Sulfoxide → Ethyl 2-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]cyclopropanecarboxylate

https://huagongshe.com/reaction/469252

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물Sodium hydrideHCID 24758—
반응물Sulfoxonium, trimethyl-, iodide (1:1)HCID 74498—
반응물ethyl (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylateHCID 66636880—
용매WaterHCID 962—
생성물Ethyl 2-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]cyclopropanecarboxylateHCID 6663698722%

반응 단계

To a 6 ml DMSO suspension of 200 mg of 60% sodium hydride was added 1.1 g of trimethylsulfoxonium iodide, followed by stirring for 30 minutes. To the reaction mixture was added 242 mg of ethyl (2E)-3-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]acrylate, followed by stirring at room temperature for 1 hour and at 60° C. for 1 hour. To the reaction mixture was added water, followed by extraction with diethyl ether. The organic layer was washed with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate, the solvent was evaporated under a reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain 55 mg of ethyl 2-[7-(cyclohexylamino)-1-cyclopentyl-6-fluoro-4-oxo-1,4-dihydroquinolin-3-yl]cyclopropanecarboxylate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629126B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-e89fa6966441413bbc453c2fcbfcb28c
출처 메모uspto-grants-2014_01