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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5460생성일: 2026년 10월 24일

Acetonitrile → 5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridine

https://huagongshe.com/ko/reaction/5460

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물TriethylamineHCID 8471—
반응물5-[3-(Amino)propyloxy]imidazo[1,2-a]pyridine dihydrochlorideHCID 23362997—
용매DichloromethaneHCID 6344—
생성물5-[3-(Benzenesulfonamido)propyloxy]imidazo[1,2-a]pyridineHCID 2336297859.5%

반응 단계

To a suspension of 5-[3-(amino)propyloxy]imidazo[1,2-a]pyridine dihydrochloride (2.64 g, 10 mmoles) and triethylamine (4.88 ml, 35 mmoles) in methylene chloride (100 ml)-acetonitrile (30 ml) was added benzenesulfonyl chloride (1.53 ml, 12 mmoles) under ice-cooling with stirring and the mixture was stirred at room temperature for 1 hour. The reaction mixture was washed in turn with an aqueous sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the crude product thus obtained was recrystallized from methylene-ethanol to obtain 1.97 g of the desired product (59.5%, light brown crystals).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05244908
출처 데이터셋uspto-grants-1993_09
ORD IDord-87ae7e60b3f94aeab00f82581b06295a
출처 메모uspto-grants-1993_09