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HRID 2303作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/2303

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US05728706
出典データセットuspto-grants-1998_03
ORD IDord-5cec6056ae4c4169bd4252bc117b2be6
出典メモuspto-grants-1998_03