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N-Benzylacetamide → 3-benzyl-7-chloro-2-methylquinazolin-4(3H)-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-Benzylacetamide | HCID 11500 | — |
| 反応物 | 2-Amino-4-chlorobenzoic acid | HCID 66646 | — |
| 溶媒 | Phosphorus oxychloride | HCID 24813 | — |
| 生成物 | 3-benzyl-7-chloro-2-methylquinazolin-4(3H)-one | HCID 58378196 | — |
反応手順
2-Amino-4-chlorobenzoic acid (250 mg, 1 eq.) and N-benzylacetamide (261 mg, 1.2 eq.) were dissolved in phosphorus oxychloride (2 ml). The reaction was placed in the microwave for 10 minutes at 150° C. The reaction was quenched by pouring the mixture into ice. The crude product was extracted into ethyl acetate. The ethyl acetate layer was washed with water, 10% aqueous sodium hydroxide, dried with magnesium sulfate, filtered, and concentrated to yield 3-benzyl-7-chloro-2-methylquinazolin-4 (3H)-one as an orange solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07939539B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-6d9d58d3257b4282bb0988a4d0392c84 |
| 出典メモ | uspto-grants-2011_05 |