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HRID 619477作成日:2026年10月26日

Putrescine → 5-[N-(4-pentafluoropropionamidobutan-1-yl)aminomethyl]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/619477

反応式

関与物質

役割名称HCID仕込み量
反応物PutrescineHCID 1045—
反応物TriethylamineHCID 8471—
反応物Pentafluoropropionic acidHCID 62356—
反応物177485-72-2HCID 21190178—
溶媒AcetonitrileHCID 6342—
生成物5-[N-(4-pentafluoropropionamidobutan-1-yl)aminomethyl]imidazo[1,2-a]pyridineHCID 21190230—

反応手順

A suspension of 15.13 g (69.69 mmol) of 5-chloromethylimidazo[1,2-a]pyridine-hydrochloride and 12.29 g (139.38 mmol) of 1,4-diaminobutane in 150 ml of acetonitrile was heated for one hour under reflux while stirring. The reaction mixture was cooled to room temperature. The resulting precipitates of 1,4-diaminobutane-dihydrochloride were filtered off. To the filtrate were added 20.61 ml (139.38 mmol) of ethyl ester of pentafluoropropionic acid and 19.43 ml (139.38 mmol) of triethylamine. The mixture was stirred for one hour at room temperature. The solvent was then distilled off under reduced pressure, and the residue was extracted with 200 ml of dichloromethane. The organic layer was washed with 150 ml of a saturated aqueous saline solution, dried over magnesium sulfate, and distilled off the solvent. The residue was purified by silica gel column chromatography (eluent; dichloromethane:methanol=20:1) to afford 13.61 g of the desired compound (53.6%, a pale yellow liquid).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05958942
出典データセットuspto-grants-1999_09
ORD IDord-7331a9ab89174fcb9fc67d2b49782f68
出典メモuspto-grants-1999_09