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Ammonia → 3,4-Dimethoxy-6-nitrobenzamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 反応物 | 4,5-Dimethoxy-2-nitrobenzoic acid | HCID 78690 | — |
| 生成物 | 3,4-Dimethoxy-6-nitrobenzamide | HCID 2736193 | — |
反応手順
4,5-Dimethoxy-2-nitrobenzoic acid (3) was treated with thionyl chloride and then reacted with ammonia to give 4,5-dimethoxy-2-nitrobenzamide (4) as described by F. Nomoto et al. Chem. Pharm. Bull., 1990, 38, 1591-1595. The nitro group in compound (4) was reduced with sodium borohydride in the presence of copper sulfate (see C.L. Thomas, Catalytic Processes and Proven Catalysts, Academic Press, New York (1970)) to give 4,5-dimethoxy-2-aminobenzamide (5) which was cyclized by refluxing with formic acid to give 6,7-dimethoxyquinazoline-4(3H)-one (6). Compound (6) was refluxed with phosphorus oxytrichloride to provide the common synthetic precursor (7).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06313130B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-8be6a258a91d45d784672c58bba29202 |
| 出典メモ | uspto-grants-2001_11 |