化工社化工社 化学情報印刷レポート · 研究参考用
1,1,1-Triethoxybutane → 1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1,1,1-Triethoxybutane | HCID 371779 | — |
| 反応物 | Pyridinium chloride | HCID 10176127 | — |
| 反応物 | N4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamine | HCID 86064731 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinoline | HCID 67203977 | 85.3% |
反応手順
Triethyl orthobutyrate (2.2 mL, 14 mmol) was added to a stirred solution of N4-{2-[2-(methylsulfonyl)ethoxy]ethyl}quinoline-3,4-diamine (3.6 g, 12 mmol) in acetonitrile (60 mL). Pyridine hydrochloride (0.3 g) was added and the reaction mixture was heated to reflux with the volatiles being collected in a Dean Stark trap. After 40 minutes analysis by TLC indicated that the starting material was consumed. The reaction mixture was concentrated under reduced pressure to provide 3.7 g of 1-{2-[2-(methylsulfonyl)ethoxy]ethyl}-2-propyl-1H-imidazo[4,5-c]quinoline as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07939526B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-a8602f05cb754a1689b7a06ba4ceaf0b |
| 出典メモ | uspto-grants-2011_05 |