戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 66351作成日:2026年10月27日

2-(3-Nitrophenyl)oxazolo[4,5-b]pyridine → 3-(Oxazolo[4,5-b]pyridin-2-yl)aniline

https://huagongshe.com/reaction/66351

反応式

関与物質

役割名称HCID仕込み量
反応物2-(3-Nitrophenyl)oxazolo[4,5-b]pyridineHCID 12461374—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物3-(Oxazolo[4,5-b]pyridin-2-yl)anilineHCID 611086—

反応手順

A mixture of 700mg. of 2-(3-nitrophenyl)oxazolo[4,5-b]pyridine in 50 ml. of ethanol was hydrogenated over 150 mg. of 5% palladium-on-carbon catalyst. The catalyst was removed by filtration and the solvent was concentrated to dryness. The residue was recrystallized from chloroform-petroleum ether to give 2-(3-aminophenyl)oxazolo[4,5-b]pyridine, m.p. 179°-180.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04131677
出典データセットuspto-grants-1978_12
ORD IDord-08c5e003bb1e44bfb83ec6053d9066fd
出典メモuspto-grants-1978_12