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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 370269생성일: 2026년 10월 26일

Cyclooctanecarbaldehyde → N-[1-(cyclooctylmethyl)piperidin-4-yl]xanthene-9-carboxamide

https://huagongshe.com/reaction/370269

반응식

참여 물질

역할이름HCID투입량
반응물CyclooctanecarbaldehydeHCID 81190—
반응물Sodium BicarbonateHCID 516892—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물N-(piperidin-4-yl)xanthene-9-carboxamide hydrochlorideHCID 23283003—
용매TetrahydrofuranHCID 8028—
생성물N-[1-(cyclooctylmethyl)piperidin-4-yl]xanthene-9-carboxamideHCID 1076519945.4%

반응 단계

1.16 g of N-(piperidin-4-yl)xanthene-9-carboxamide hydrochloride and 586 mg of cyclooctanecarbaldehyde were suspended in 60 ml of tetrahydrofuran 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, followed by drying over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, the obtained residue was purified by silica gel column chromatography (developing solvent: chloroform--chloroform/methanol=50/1), and 660 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-9d8f9799d59b4fccaab715570a02b422
출처 메모uspto-grants-2000_10