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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2047704생성일: 2026년 10월 26일

1-Iodo-3-methylbutane → 6-(3-Chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5-(3-methyl-butyl)-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2047704

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참여 물질

역할이름HCID투입량
반응물1-Iodo-3-methylbutaneHCID 10924—
반응물Sodium hydrideHCID 24758—
반응물HCID 66587522HCID 66587522—
용매DimethylformamideHCID 6228—
생성물6-(3-Chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5-(3-methyl-butyl)-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl esterHCID 6658770573.9%

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온도0 °C

반응 단계

To a 0° C. solution of 6-(3-chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester (200 mg, 0.5 mmol) in N,N-dimethylformamide (5 mL) was added a 60% dispersion of sodium hydride in mineral oil (44 mg, 1.1 mmol) portionwise. The mixture was stirred at 0° C. for 30 min and then 1-iodo-3-methyl-butane (327 mg, 1.6 mmol) was added to above mixture dropwise at 0° C. The mixture was stirred at 0° C. for 3 hours and then extracted with ethyl acetate, washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The yellowish residue was purified by ISCO combi-flash chromatography (gradient elution, 0-5% ethyl acetate/hexane) to afford 6-(3-chloro-4-fluoro-phenyl)-8-ethyl-8-methyl-5-(3-methyl-butyl)-5,6,7,8-tetrahydro-[1,5]naphthyridine-2-carboxylic acid methyl ester (160 mg, 67.5%) as a yellow oil. MS (ESI+) [(M+H)+] 433.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08592594B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-94d32a24d5124111b84cf2d5c19ac397
출처 메모uspto-grants-2013_11