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HRID 1267313作成日:2026年10月26日

Ethyl Acetate → 5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine

https://huagongshe.com/reaction/1267313

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物2-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy)-5-nitropyridineHCID 11067329—
触媒HCID 178418390HCID 178418390—
溶媒MethanolHCID 887—
生成物5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridineHCID 1108772293.7%

反応手順

A mixture of 2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-nitropyridine (13.4 g), palladium-carbon (5%, 1.5 g) and ethyl acetate (200 ml)-methanol (150 ml) was subjected catalytic hydrogenation at room temperature under one atmospheric pressure. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residual crystals were collected by filtration to obtain 5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (11.4 g, 93%). Recrystallization from ethyl acetate-hexane gave brown crystals, m.p.107.0-108.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06552058B1
出典データセットuspto-grants-2003_04
ORD IDord-0c1aaefdf7914842988a2268d63fd681
出典メモuspto-grants-2003_04