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HRID 1377650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/1377650

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US05665748
出典データセットuspto-grants-1997_09
ORD IDord-8878d59c325e49e29ce1f4d458b795da
出典メモuspto-grants-1997_09