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HRID 1082299作成日:2026年10月26日

2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol → 2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanol

https://huagongshe.com/reaction/1082299

反応式

関与物質

役割名称HCID仕込み量
反応物2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanolHCID 11807790—
触媒HCID 178418390HCID 178418390—
溶媒EthanolHCID 702—
生成物2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanolHCID 1111829789.7%

反応手順

A mixture of 2-{6-azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (19.6 g), 10% palladium-carbon (50% moist) (4.0 g) and ethanol (240 ml) is subjected to catalytic hydrogenation at room temperature under hydrogen atmosphere (1 atm) for one hour. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is recrystallized from ethyl acetate/n-hexane to give 2-{6-amino-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (15.9 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05589478
出典データセットuspto-grants-1996_12
ORD IDord-938db4b6a7e84b90807c1255f7dfd655
出典メモuspto-grants-1996_12