戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 4731作成日:2026年10月24日

Potassium Hydroxide → 3-(4-Dibutylaminopropoxybenzoyl)-8-methylimidazo[1,2-a]pyridine

https://huagongshe.com/ja/reaction/4731

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物N-(3-Chloropropyl)dibutylamineHCID 96084—
反応物3-(4-Hydroxybenzoyl)-8-methylimidazo[1,2-a]pyridineHCID 14201455—
溶媒MethanolHCID 887—
生成物3-(4-Dibutylaminopropoxybenzoyl)-8-methylimidazo[1,2-a]pyridineHCID 10273738—

反応手順

A mixture of 3-(4-hydroxybenzoyl)-8-methylimidazo[1,2-a]-pyridine (2.3 g, 9.6 mmol), dibutylaminopropyl chloride (6.8 g, 33 mmol) and potassium hydroxide (1.3 g, 23 mmol) in methanol (60 ml) was stirred at reflux for 96 hours. The mixture was concentrated and the resulting oil was flash chromatographed (silica gel, 2.5% methanol in diethyl ether) to give 1.3 g (31% yield) of the free base of the title compound. The HCl salt was prepared by dropwise addition of concentrated hydrochloric acid to a solution of the free base in methanol, concentrated and recrystallized from acetone-ether to give the HCl salt of the title compound as an off-white solid, mp 105° C. to 107° C. lR(KBr): 3440, 2640, 1645, 1605 cm-1. MS: 421 (M+). 1H NMR (CD3OD): δ9.66 (d, J=8 Hz, 1H), 8.74 (s, 1H), 8.00-7.61 (m, 4H), 7.20 (d, J=7.2 Hz, 2H), 4.29 (t, J=5 Hz, 2H), 3.41-3.15 (m, 6H), 2.75 (s, 3H), 2.31 (m, 2H), 1.80-1.42 (m, 8H), 1.02 (m, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04727145
出典データセットuspto-grants-1988_02
ORD IDord-79b7e20c21f04bd287a87a9adaed0cfb
出典メモuspto-grants-1988_02