関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | 3-Nitrophenol | HCID 11137 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 4-chloro-5,6-dimethyl-7H-pyrrolo(2,3-d)pyrimidine | HCID 13041144 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 4-(3-Nitrophenoxy)-5,6-dimethyl-7H-pyrrolo[2,3-d]-pyrimidine | HCID 58931145 | 46.9% |
反応手順
After adding 3-nitrophenol (243 mg), potassium carbonate (268 mg) and dimethylformamide (2 ml) to the 4-chloro-5,6-dimethyl-7H-pyrrolo[2,3-d]-pyrimidine (177 mg) described in Journal of Medicinal Chemistry, 1996, Vol. 39, No. 12, 2285-2292, the mixture was stirred at 120-130° C. for 72 hours. This was returned to room temperature, water was added, extraction was performed with a tetrahydrofuran and ethyl acetate mixed solution, and then the organic layer was washed with saturated saline, dried over anhydrous sodium sulfate and concentrated to dryness. The obtained crystals were washed with diethyl ether to obtain the title compound (130 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08372981B2 |
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| 出典データセット | uspto-grants-2013_02 |
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| ORD ID | ord-63b0879abf924eaabe53a54cd990fcb0 |
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| 出典メモ | uspto-grants-2013_02 |
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