関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2,4-Dimethoxybenzonitrile | HCID 77750 | — |
| 反応物 | 4,5-Diaminopyrimidine | HCID 83703 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | 1H-Purine, 8-(2,4-dimethoxyphenyl)- | HCID 3059912 | — |
反応手順
A mixture of 2 g of 4,5-diamino-pyrimidine, 4 g of 2,4-dimethoxy-benzonitrile, 6 g of p-toluene sulfonic acid hydrate, and 40 ml of benzene was heated, whereby the benzene was distilled off. The residue was heated for 30 minutes at 120° C. After cooling the residue was triturated with 2 N ammonia and extracted with ethyl acetate. The ethyl acetate phase was extracted with 2 N hydrochloric acid, the aqueous phase was neutralized and again extracted with ethyl acetate, and subsequently the organic phase was extracted with 2 N sodium hydroxide solution. When the aqueous phase was neutralized, the product was precipitated and recrystallized from water.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04299834 |
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| 出典データセット | uspto-grants-1981_11 |
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| ORD ID | ord-63f0d60977ab4bd0987398e8ee4f424a |
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| 出典メモ | uspto-grants-1981_11 |
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