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HRID 1011047作成日:2026年10月25日

Potassium Carbonate → N2-(2-Cyclopropylethyl)-8-(methyloxy)-9-(tetrahydro-2H-pyran-3-ylmethyl)-9H-purine-2,6-diamine

https://huagongshe.com/reaction/1011047

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Tetrahydro-2H-pyran-3-ylmethyl methanesulfonateHCID 22402475—
反応物N2-(2-Cyclopropylethyl)-8-(methoxy)-9H-Purine-2,6-diamine trifluoroacetateHCID 178493988—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N2-(2-Cyclopropylethyl)-8-(methyloxy)-9-(tetrahydro-2H-pyran-3-ylmethyl)-9H-purine-2,6-diamineHCID 5769957588%

反応条件

温度60 °C

反応手順

To a solution of N2-(2-cyclopropylethyl)-8-(methoxy)-9H-purine-2,6-diamine trifluoroacetate (400 mg) in N,N-dimethylformamide (6.90 ml) at room temperature was added potassium carbonate (610 mg) and the reaction stirred at 60° C. for 90 minutes. The reaction mixture was cooled to room temperature and tetrahydro-2H-pyran-3-ylmethyl methanesulfonate (236 mg) was added. Stirring was continued at 50° C. for 20 hours. The reaction temperature was increased to 90° C. and stirring continued. The reaction was cooled and taken up in ethyl acetate (50 ml) and washed with water (2×50 ml). The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo to give an orange oil. The product was purified by C18 reverse phase chromatography using water (containing 0.1% formic acid)-acetonitrile (containing 0.05% formic acid) as eluant (10-50%) to afford the title compound as a colourless oil (198 mg, 88% pure).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07977344B2
出典データセットuspto-grants-2011_07
ORD IDord-be4bc315c52b41e5bcdb534c7b347c54
出典メモuspto-grants-2011_07