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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370272생성일: 2026년 10월 25일

Cyclooctanecarbaldehyde → N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamide

https://huagongshe.com/reaction/370272

반응식

참여 물질

역할이름HCID투입량
반응물CyclooctanecarbaldehydeHCID 81190—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-(9-azabicyclo[3.3.1]nonan-3-yl)xanthene-9-carboxamide hydrochlorideHCID 23283000—
용매MethanolHCID 887—
생성물N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamideHCID 1548066919%

반응 단계

38.5 mg of N-(9-azabicyclo[3.3.1]nonan-3-yl)xanthene-9-carboxamide hydrochloride and 44.1 mg of cyclooctanecarbaldehyde were suspended in 3 ml of methanol at room temperature, and 1.60 g of sodium triacetoxyborohydride was added thereto, followed by stirring for 12 hours at the same temperature. Saturated aqueous sodium bicarbonate was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with saturated aqueous sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by preparative thin layer chromatography (Kieselgel™60F254, Art5744 produced by Merck Co.: chloroform/methanol=19/1), and 9.0 mg of the title compound as a white solid was obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06140338
출처 데이터셋uspto-grants-2000_10
ORD IDord-579a5cdcf625477db273cebaf834e15b
출처 메모uspto-grants-2000_10