関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethoxyacetyl chloride | HCID 84189 | — |
| 反応物 | 1-[2-(3-Amino-7-bromoquinolin-4-ylamino)ethyl]-3-(2-methylethyl)urea | HCID 21984426 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1-[2-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-3-(2-methylethyl)urea | HCID 21984285 | — |
反応手順
To a stirred solution of 1-[2-(3-amino-7-bromoquinolin-4-ylamino)ethyl]-3-(2-methylethyl)urea (27.2 g, 0.0743 mol) in 600 mL pyridine was slowly added ethoxyacetyl chloride (1.1 equivalents). After 1.5 hours the mixture was yellow and turbid. The reaction mixture was then heated at 80° C. for 12 hours and then concentrated under reduced pressure. The residue was dissolved in water and saturated aqueous potassium carbonate and stirred vigorously for three hours. A precipitate was present, was isolated by filtration, and air-dried for 48 hours to provide 32 g of 1-[2-(7-bromo-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-3-(2-methylethyl)urea.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091214B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-9312b9100a3448fd880c4a1e4f95c690 |
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| 出典メモ | uspto-grants-2006_08 |
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