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Quinoline-3-carboxylic acid → N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoline-3-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Quinoline-3-carboxylic acid | HCID 80971 | — |
| 反応物 | 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 22180872 | — |
| 生成物 | N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoline-3-carboxamide | HCID 10322391 | 28.5% |
反応手順
Using the general method of Example 181 1-(4-aminobutyl)-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-4-amine (2.0 g, 6.37 mmol) was reacted with quinoline-3-carboxylic acid (1.33 g, 7.66 mmol) to provide 850 mg of N-{4-[4-amino-2-(2-methoxyethyl)-1H-imidazo[4,5-c]quinolin-1-yl]butyl}quinoline-3-carboxamide as a yellow solid, m.p. 114-116° C. Analysis: Calculated for C27H28N6O2.0.2 H2O: % C, 68.68; % H, 6.06; % N, 17.80. Found: % C, 68.68; % H, 5.85; % N, 17.76.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06756382B2 |
| 出典データセット | uspto-grants-2004_06 |
| ORD ID | ord-96251fd2503944d59d419f32de1ad0f2 |
| 出典メモ | uspto-grants-2004_06 |