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HRID 44986作成日:2026年10月25日

Morpholine → 4-(5-Bromopyridin-3-yl)morpholine

https://huagongshe.com/reaction/44986

反応式

関与物質

役割名称HCID仕込み量
反応物MorpholineHCID 8083—
反応物1,4-DioxaneHCID 31275—
反応物3,5-DibromopyridineHCID 69369—
反応物Sodium t-butoxideHCID 23676156—
触媒HCID 178418397HCID 178418397—
生成物4-(5-Bromopyridin-3-yl)morpholineHCID 4673961441.1%

反応条件

温度80 °C

反応手順

To a solution of [3,5-dibromopyridine (1000 mg, 0.004 mol) in 1,4-dioxane (8 mL, 0.1 mol), morpholine (400 mg, 0.004 mol) and sodium tert-butoxide (400 mg, 0.004 mol) were added. The reaction was bubbled with nitrogen. Tetrakis(triphenylphosphine)palladium(0) (200 mg, 0.0002 mol) was added and nitrogen was bubbled through for couple of minutes. The mixture was heated at 80° C. overnight. The reaction was allowed to cool to rt and was then partitioned between water and ethyl acetate. The organic layer was washed with saturated sodium chloride, dried over magnesium sulfate, filtered and concentrated to give a crude residue. The crude product was purified by FCC on silica gel eluting with 1:1, EtOAC:Hexane gave to give 4-(5-bromopyridin-3-yl)morpholine as a viscous oil (400 mg, 40%). 1H NMR (400 MHz, CDCl3): 8.2 (s, 1H), 8.1 (s, 1H), 7.2 (s, 1H), 3.8 (m, 4H), 3.2 (m, 4H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541425B2
出典データセットuspto-grants-2013_09
ORD IDord-f68c61ed84274e17b1717f97a24de537
出典メモuspto-grants-2013_09