関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-Amino-3,4-dimethoxybenzonitrile | HCID 18778990 | — |
| 反応物 | Ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochloride | HCID 20506452 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline | HCID 12920014 | — |
反応手順
To a stirred solution of 1.78 g. (0.01 mole) 3,4-dimethoxy-2-aminobenzonitrile in 30 ml. of N,N-dimethylformamide is added 2.88 g. (0.01 mole) ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochloride followed by 855 mg. (0.02 mole) of a 56.1% dispersion of sodium hydride in mineral oil. The reaction mixture is stirred at ambient temperature for 30 minutes, and then it is heated to ca. 100° C. and maintained at that temperature for 12 hours. The reaction mixture is cooled to ambient temperature, diluted with an excess of water, and then extracted with chloroform. The chloroform extract is washed several times with water, dried using anhydrous magnesium sulfate, and then evaporated to dryness in vacuo. This affords crude 7,8-dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline, which is purified further by recrystallization from aqueous ethanol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04351940 |
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| 出典データセット | uspto-grants-1982_09 |
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| ORD ID | ord-662e012e42b440e49cc52795ac9bde36 |
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| 出典メモ | uspto-grants-1982_09 |
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