関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Valeryl chloride | HCID 61186 | — |
| 反応物 | 2-Amino-5-methylbenzoic acid | HCID 76255 | — |
| 反応物 | Ethyl acetate hexane | HCID 21226206 | — |
| 触媒 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | HCID 178441839 | HCID 178441839 | 25% |
反応手順
To a solution of 3.0 g (20 mmol) of 2-amino-5-methyl benzoic acid in 20 mL of dry DMF at 0° C. was added 200 mg of DMAP followed by 6.07 g (60 mmol) of triethylamine and 5.02 g (40 mmol) of valeryl chloride. The resulting mixture was stirred at 0° C. for 30 min. The mixture was heated to 110° C. and monitored by TLC for the formation of the intermediate quinoxazolone (Rf =0.8, 40% EtOAc/hexane). Following complete formation of the intermediate 10 g (100 mmol) of (NH4)2CO3 was added cautiously. Heating was continued to ensure consumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one. The reaction mixture was concentrated in vacuo and the residue was taken up in 50 mL of ether and 50 mL of water. The mixture was filtered and the filtrate discarded after washing the residue with 20 mL of ether. The residue was recrystalized from MeOH to give 1.07 g (25%) of the title compound as a white crystalline solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05401745 |
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| 出典データセット | uspto-grants-1995_03 |
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| ORD ID | ord-c212d50860dd4e1982e2f03aeb761ec5 |
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| 出典メモ | uspto-grants-1995_03 |
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