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4-Quinolinecarbonyl chloride → N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]4-quinolinecarboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Quinolinecarbonyl chloride | HCID 9990126 | — |
| 反応物 | 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 15453775 | — |
| 生成物 | N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]4-quinolinecarboxamide | HCID 12144530 | — |
反応手順
According to the general method of Example 14, 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin4-amine and quinoline4-carbonyl chloride were combined to provide N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]4-quinolinecarboxamide as a white crystalline solid, m.p. 214.5-215.2° C. 1H NMR (300 MHz, DMSO-d6) δ 8.89 (d, J=4.3 Hz, 1H), 8.76 (t, J=5.6 Hz, 1H), 8.24 (s, 1H), 8.10-8.01 (m, 3H), 7.78 (ddd, J=8.4, 6.9, 1.5 Hz, 1H), 7.64 (dd, J=8.4, 1.1 Hz, 1H), 7.56 (ddd, J=8.3, 6.9, 1.4 Hz, 1H), 7.44 (ddd, J=8.3, 7.0, 1.3 Hz, 1H), 7.34 (d, J=4.3 Hz, 1H), 7.24 (ddd, J=8.3, 7.0, 1.3 Hz, 1H), 6.60 (broad s, 2H), 4.68 (t, J=6.9 Hz, 2H), 3.38 (q, J=7.0 Hz, 2H), 2.00 (m, 2H), 1.63 (m, 2H); MS (EI) m/e 410.1860 (410.1855 calcd for C24H22N6O).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07393859B2 |
| 出典データセット | uspto-grants-2008_07 |
| ORD ID | ord-4056689d51454421872bb83ffab53864 |
| 出典メモ | uspto-grants-2008_07 |