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HRID 20074作成日:2026年10月25日

4-Bromopyridine → Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/20074

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromopyridineHCID 14268—
反応物Ethyl 4-amino-1-piperidinecarboxylateHCID 100867—
反応物Binap, (A+-)-HCID 634876—
反応物Sodium t-butoxideHCID 23676156—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物Ethyl 4-(pyridin-4-ylamino)piperidine-1-carboxylateHCID 2229322341.1%

反応手順

A solution of ethyl 4-aminopiperidine-1-carboxylate (2.20 g, 12.7 mmol), 4-bromopyridine (3.47 g, 17.8 mmol), sodium t-butoxide (4.54 g, 47.2 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.398 g, 0.639 mmol) and palladium acetate (0.143 g, 0.639 mmol) in toluene (40 mL) was heated at 60° C. overnight. The reaction was cooled and partitioned between ethyl acetate and water. The aqueous layer was washed 3 times with methylene chloride, and the combined organic layers dried over sodium sulfate. The crude product was purified by chromatography (silica gel, 0 to 10% {5% ammonium hydroxide in methanol}in methylene chloride gradient elution), which gave the title compound (1.3 g, 41% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745427B2
出典データセットuspto-grants-2010_06
ORD IDord-101a650b45d542b081d56e34c403fdfc
出典メモuspto-grants-2010_06