関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Methoxybenzylamine | HCID 75452 | — |
| 反応物 | 4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrile | HCID 2777510 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile | HCID 5200312 | 25.1% |
反応手順
4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (example 72) (0.66 g, 3.23 mmol) was suspended in DMF (7 mL), and 4-methoxybenzylamine (0.94 mL, 7.26 mmol) was added. The reaction was heated at 100° C. for 1 hour and the DMF was removed under vacuum. The residue was dissolved in TFA (6 mL) and stirred at room temperature for 30 minutes and dichloromethane (10 mL) was added. The solid product that formed was collected, suspended in water and the solution stirred overnight. The solid was collected by filtration to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.150 g, 25%) as a white solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ 7.19 (m, 2H), 7.57 (m, 1H), 7.88 (bs, 2H), 8.12 (d, J=7.6 Hz, 1H), 11.23 (s, 1H). MS 186 (MH+).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08633186B2 |
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| 出典データセット | uspto-grants-2014_01 |
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| ORD ID | ord-27a81234d9524a9da815197b3a778c23 |
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| 出典メモ | uspto-grants-2014_01 |
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