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HRID 2315作成日:2026年10月25日

Sodium hydride → 5-Bromo-6-[2-(5-methylthiopyrimidin-2-yloxy)ethoxy]pyrimidine-4-amine

https://huagongshe.com/reaction/2315

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-(6-Amino-5-bromopyrimidin-4-yloxy)ethanolHCID 18931106—
反応物2-Chloro-5-(methylthio)pyrimidineHCID 21979532—
溶媒DimethylformamideHCID 6228—
生成物5-Bromo-6-[2-(5-methylthiopyrimidin-2-yloxy)ethoxy]pyrimidine-4-amineHCID 1968952553.6%

反応手順

To a solution of 2-(6-amino-5-bromopyrimidin-4-yloxy)ethanol (611 mg) in dimethylformamide (20 ml) is added sodium hydride (60% dispersion-type, 125 mg), and the mixture is stirred for 20 minutes. To the mixture is added 2-chloro-5-methylthiopyrimidine (461 mg), and the mixture is stirred at room temperature for three hours. To the mixture is added ice-water, and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed, dried, and evaporated to remove the solvent. The residue is purified by silica get column chromatography (solvent; chloroform/methanol=20:1), and crystallized from ethyl acetate/diisopropyl ether to give 5-bromo-6-[2-(5-methythiopyrimidin-2-yloxy)ethoxy]pyrimidine-4-amine (501 mg).

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-4bd91debc1224985b59b17dd05823067
出典メモuspto-grants-1998_03