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HRID 10436作成日:2026年10月26日

Sodium methanethiolate → N-(2,2-diphenylethyl)-2-(methylsulphanyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amine

https://huagongshe.com/reaction/10436

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium methanethiolateHCID 4378561—
反応物2-Chloro-N-(2,2-diphenylethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amineHCID 10181335—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物N-(2,2-diphenylethyl)-2-(methylsulphanyl)-9-tetrahydro-2H-pyran-2-yl-9H-purin-6-amineHCID 2197827799.8%

反応条件

温度100 °C

反応手順

A solution of 2-chloro-N-(2,2-diphenylethyl)-9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-amine (Preparation 2) (49.7 g, 0.11 mol) in dry N,N-dimethylformamide (200 ml) was treated with sodium thiomethoxide (10 g, 0.14 mol) and the resulting mixture heated under an atmosphere of nitrogen at 100° C. for 90 minutes. The mixture was stirred at room temperature for 72 hours and then reheated at 100° C. for a further 2 hours. The reaction mixture was cooled and diluted with water (1000 ml). A suspension was formed which was extracted with diethyl ether (×2). The combined organic layers were washed sequentially with water and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was azeotroped with diethyl ether followed by pentane to afford the title compound as a foam (48.9 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094769B2
出典データセットuspto-grants-2006_08
ORD IDord-0158caa0433b4a16981a9e69a7155cdb
出典メモuspto-grants-2006_08