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Ethoxyacetyl chloride → 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethoxyacetyl chloride | HCID 84189 | — |
| 反応物 | 7-bromo-N4-isobutylquinoline-3,4-diamine | HCID 68818159 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline | HCID 21984386 | 41.1% |
反応手順
A solution of 7-bromo—N4-isobutylquinoline-3,4-diamine (85 g, prepared according to Part F of Example 1) in anhydrous pyridine (413 mL) was immersed in an ice bath, and ethoxyacetyl chloride (36.9 g, 300 mmol) was added. The reaction was allowed to warm to room temperature and was then heated in an oil bath held at 85° C. for 3.5 h. The reaction mixture was concentrated under vacuum, and the residue was taken up in diethyl ether and washed with 2M Na2CO3 (2×) followed by H2O (1×). The organic layer was dried (MgSO4), filtered, and concentrated. Recrystallization of the resulting solid from boiling 15% ethyl acetate in hexanes afforded 43.0 g of 7-bromo-2-ethoxymethyl-1-isobutyl-1H-imidazo[4,5-c]quinoline as brown crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07091214B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-dbeb3e2c5d2e43e88e3b4fdfc8b56049 |
| 出典メモ | uspto-grants-2006_08 |