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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Tetrahydro-2H-pyran-3-ylmethyl methanesulfonate | HCID 22402475 | — |
| 反応物 | N2-(2-Cyclopropylethyl)-8-(methoxy)-9H-Purine-2,6-diamine trifluoroacetate | HCID 178493988 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N2-(2-Cyclopropylethyl)-8-(methyloxy)-9-(tetrahydro-2H-pyran-3-ylmethyl)-9H-purine-2,6-diamine | HCID 57699575 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07977344B2 |
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| 出典データセット | uspto-grants-2011_07 |
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| ORD ID | ord-be4bc315c52b41e5bcdb534c7b347c54 |
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| 出典メモ | uspto-grants-2011_07 |
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