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HRID 1357708作成日:2026年10月26日
N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide → 6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline Dihydrochloride
https://huagongshe.com/reaction/1357708
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide | HCID 17904941 | — |
| 反応物 | 4-Chloro-7-methoxyquinazolin-6-yl acetate--hydrogen chloride (1/1) | HCID 22022159 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 6-Acetoxy-7-methoxy-4-[2-methyl-5-(2-morpholinopyridine-4-carboxamido)anilino]quinazoline Dihydrochloride | HCID 22732247 | 80% |
反応手順
A mixture of N-(3-amino-4-methylphenyl)-2-morpholinopyridine-4-carboxamide (178 mg), 6-acetoxy-4-chloro-7-methoxyquinazoline hydrochloride (150 mg) and isopropanol (5 ml) was stirred and heated to 85° C. for 3 hours. The reaction mixture was allowed to cool to ambient temperature and the solid was isolated and washed in turn with isopropanol (5 ml) and isohexane (2×5 ml). There was thus obtained the title compound (249 mg, 80%); NMR: 2.17 (s, 3H), 2.38 (s, 3H), 3.56 (m, 4H), 3.72 (m, 4H), 4.0 (s, 3H), 7.16 (m, 1H), 7.37 (m, 2H), 7.52 (s, 1H), 7.68 (m, 1H), 7.87 (m, 1H), 8.24 (m, 1H), 8.67 (s, 1H), 8.8 (s, 1H), 10.6 (s, 1H), 11.50 (s, 1H); m/s: M+H+ 529.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06593333B1 |
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| 出典データセット | uspto-grants-2003_07 |
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| ORD ID | ord-e3fbb0c15761475b9c44c4750f971983 |
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| 出典メモ | uspto-grants-2003_07 |
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