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HRID 513751作成日:2026年10月25日

Hydrogen Bromide → 1,5-Naphthyridin-4-amine

https://huagongshe.com/reaction/513751

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Sodium BicarbonateHCID 516892—
反応物(4-Methoxy-benzyl)-[1,5]naphthyridin-4-yl-amineHCID 68183180—
生成物AmmoniaHCID 222—
生成物1,5-Naphthyridin-4-amineHCID 589354183.2%

反応条件

温度80 °C

反応手順

48% HBr (13 ml) was added to (4-methoxy-benzyl)-[1,5]naphthyridin-4-yl-amine 485 (0.5 g, 1.88 mmol) and the mixture was heated at 80° C. for 2 h. After cooling, the mixture was neutralized with sat. NaHCO3 solution and the aqueous phase was extracted with EtOAc (80 ml). The organic phase was washed with water, dried (Na2SO4) and concentrated in vacuo. The crude residue was purified by column chromatography with DCM/MeOH/Aq. NH3 (97:2:1) as the eluent to give the title compound (0.25 g, 90%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09102688B2
出典データセットuspto-grants-2015_08
ORD IDord-1c2a075070054a5a80d59412cb89a2be
出典メモuspto-grants-2015_08