戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1818215作成日:2026年10月23日

Pyrazole → 2-ethoxymethyl-1-(3-methoxypropyl)-7-(pyrazol-1-yl)-1H-imidazo[4,5-c]quinolin-4-amine

https://huagongshe.com/ja/reaction/1818215

反応式

関与物質

役割名称HCID仕込み量
反応物PyrazoleHCID 1048—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物7-bromo-2-ethoxymethyl-1-(3-methoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 21984070—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒1,4-DioxaneHCID 31275—
生成物2-ethoxymethyl-1-(3-methoxypropyl)-7-(pyrazol-1-yl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 2198428125%

反応手順

A 4 dram vial containing a stir bar was charged sequentially with copper(I) iodide (0.003 g), potassium phosphate (0.890 g), pyrazole (0.164 g), 7-bromo-2-ethoxymethyl-1-(3-methoxypropyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.786 g), (1)-trans-1,2-diaminocyclohexane (0.030 mL), and anhydrous 1,4-dioxane (2 mL). The vial was flushed with nitrogen, capped, and placed in an oil bath at 110° C. After 15.5 hours, the reaction was cooled to room temperature and purified by flash column chromatography using a gradient of CMA/chloroform as the eluent. Subsequent recrystallization from acetonitrile yielded 0.190 g of 2-ethoxymethyl-1-(3-methoxypropyl)-7-(pyrazol-1-yl)-1H-imidazo[4,5-c]quinolin-4-amine as a white solid, mp 159.0-160.0° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598382B2
出典データセットuspto-grants-2009_10
ORD IDord-1effe6cf34cd45f0aacc9490cce500fa
出典メモuspto-grants-2009_10