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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1947131생성일: 2026년 10월 27일

Sodium Iodide → N-{2-[ethyl(2-hydroxyethyl)amino]ethyl}-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamide

https://huagongshe.com/reaction/1947131

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물DiisopropylethylamineHCID 81531—
반응물EthylaminoethanolHCID 18179409—
반응물N-(2-chloroethyl)-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamideHCID 66893214—
용매1-ButanolHCID 263—
용매Sodium BicarbonateHCID 516892—
생성물N-{2-[ethyl(2-hydroxyethyl)amino]ethyl}-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamideHCID 5786004435.7%

반응 단계

A solution of the obtained N-(2-chloroethyl)-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamide (200 mg, 0.43 mmol), N-ethylaminoethanol (228 mg, 2.55 mmol), diisopropylethylamine (330 mg, 2.55 mmol) and sodium iodide (64 mg, 0.43 mmol) in 1-butanol (5 mL) was stirred at 110° C. for 18 hr. The reaction mixture was diluted with saturated sodium hydrogen carbonate solution, and extracted twice with ethyl acetate. The extract was combined, washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by aminosilica gel chromatography (eluate; ethyl acetate to ethyl acetate/methanol=20/1) to give N-{2-[ethyl(2-hydroxyethyl)amino]ethyl}-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamide (0.08 g) as a white non-crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08399449B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-d0b7c70b85434e81a27e4d0ccaf93e95
출처 메모uspto-grants-2013_03