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Diallylamine → 2-Allylamino-7-methyl-4-(4-methylpiperidino)thieno[3,2-d]pyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diallylamine | HCID 31279 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-Chloro-7-methyl-4-(4-methylpiperidino)thieno[3,2-d]pyrimidine | HCID 18326464 | — |
| 生成物 | 2-Allylamino-7-methyl-4-(4-methylpiperidino)thieno[3,2-d]pyrimidine | HCID 18326440 | 43.9% |
反応手順
In a sealed tube were heated 422 mg (1.5 mmol) of 2-chloro-7-methyl-4-(4-methylpiperidino)thieno[3,2-d]pyrimidine and 1.37 g (24.0 mmol) of diallylamine at 160° C. for 16 hours. After completion of the reaction, the reaction mixture was allowed to resume room temperature, and a saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with ethyl acetate (50 ml×2). The organic layer was washed with brine and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane=1/6) to give 198 mg (yield: 43.9%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06339089B2 |
| 出典データセット | uspto-grants-2002_01 |
| ORD ID | ord-98faa77348024368bf2e13a6cd0cd3e0 |
| 出典メモ | uspto-grants-2002_01 |