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HRID 10526作成日:2026年10月26日

tert-Butyl 4-oxopiperidine-1-carboxylate → 1-Boc-4-(aminomethyl)piperidine

https://huagongshe.com/reaction/10526

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
反応物Methylamine hydrochlorideHCID 6364545—
触媒Platinum oxide (PtO)HCID 82844—
溶媒MethanolHCID 887—
生成物1-Boc-4-(aminomethyl)piperidineHCID 73681793.9%

反応手順

A solution of methylamine hydrochloride (1.01 g, Wako Pure Chemical Industries) and 1-(tert-butoxycarbonyl)-4-oxopiperidine (1.99 g, Aldrich) in methanol (13 ml) was stirred in the presence of platinum oxide (69 mg, Wako Pure Chemical Industries) at room temperature for 3 hours under hydrogen atmosphere of ordinary pressure. The hydrogen was purged with a nitrogen gas, and the platinum catalyst was removed by filtration. Then, the reaction mixture was adjusted to pH of from 10 to 11 with 1 N aqueous sodium hydroxide. The reaction mixture was added with water (10 ml), and the product was extracted three times with ethyl acetate (15 ml for each time). The organic layer was dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=20:1) to obtain the title compound (2.01 g).

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-d468fd2f35634bbfb59c0f3c2c17ef5c
出典メモuspto-grants-2006_08