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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4731생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물N-(3-Chloropropyl)dibutylamineHCID 96084—
반응물3-(4-Hydroxybenzoyl)-8-methylimidazo[1,2-a]pyridineHCID 14201455—
용매MethanolHCID 887—
생성물3-(4-Dibutylaminopropoxybenzoyl)-8-methylimidazo[1,2-a]pyridineHCID 10273738—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04727145
출처 데이터셋uspto-grants-1988_02
ORD IDord-79b7e20c21f04bd287a87a9adaed0cfb
출처 메모uspto-grants-1988_02