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HRID 370269作成日:2026年10月27日

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

https://huagongshe.com/reaction/370269

反応式

関与物質

役割名称HCID仕込み量
反応物CyclooctanecarbaldehydeHCID 81190—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物N-(piperidin-4-yl)xanthene-9-carboxamide hydrochlorideHCID 23283003—
溶媒TetrahydrofuranHCID 8028—
生成物N-[1-(cyclooctylmethyl)piperidin-4-yl]xanthene-9-carboxamideHCID 1076519945.4%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06140338
出典データセットuspto-grants-2000_10
ORD IDord-9d8f9799d59b4fccaab715570a02b422
出典メモuspto-grants-2000_10