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HRID 10531作成日:2026年10月23日

Tetramethyltin → 4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidine

https://huagongshe.com/ja/reaction/10531

反応式

関与物質

役割名称HCID仕込み量
反応物TetramethyltinHCID 11661—
反応物2,6-Di-tert-butyl-4-methylphenolHCID 31404—
反応物4-(4-Bromo-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979972—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物4-(4-Methyl-5-isoquinolyl)amino-1-(tert-butoxycarbonyl)piperidineHCID 21979807—

反応条件

温度150 °C

反応手順

A solution of Intermediate 71 (313 mg) in toluene (6 ml) was added with tetrakis(triphenylphosphine)palladium(0) (17.9 mg, Aldrich), tetramethyltin (165 μl, Kanto Chemicals) and 2,6-di-tert-butyl-4-methylphenol (several pellets, Tokyo Kasei Kogyo) and stirred in a sealed tube at 150° C. for 48 hours. The reaction mixture was cooled to room temperature, filtered through Celite and concentrated under reduced pressure. The residue was added with saturated brine (30 ml) and extracted three times with ethyl acetate (30 ml for each time). The organic layers were combined and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=2:1) to obtain the title compound (61.7 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094789B2
出典データセットuspto-grants-2006_08
ORD IDord-2e9115487cd940a38efae8fd5e24df8a
出典メモuspto-grants-2006_08