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HRID 1891239생성일: 2026년 10월 24일

Tetrabutylammonium Fluoride → {3-[2-(2,4-Difluorophenyl)-3-methylimidazo[1,2-alpha]pyridin-6-yl]phenyl}methanol

https://huagongshe.com/ko/reaction/1891239

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물6-[3-(tert-Butyldimethylsilanyloxymethyl)phenyl]-2-(2,4-difluorophenyl)-3-methylimidazo[1,2-a]pyridineHCID 69810477—
용매TetrahydrofuranHCID 8028—
생성물{3-[2-(2,4-Difluorophenyl)-3-methylimidazo[1,2-alpha]pyridin-6-yl]phenyl}methanolHCID 4423376782.1%

반응 단계

210 mg of 6-[3-(tert-butyldimethylsilanyloxymethyl)phenyl]-2-(2,4-difluorophenyl)-3-methylimidazo[1,2-α]pyridine in 5 ml of tetrahydrofuran are placed in a round-bottomed flask and 240 mg of tetrabutylammonium fluoride are added thereto. The mixture is stirred at ambient temperature for 48 h. The reaction mixture is then concentrated under reduced pressure. The residue is purified by silica gel chromatography, elution being carried out with a dichloromethane/methanol mixture. 130 mg of compound are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08507520B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-5127ccf1189a46d58465fd58b87a1788
출처 메모uspto-grants-2013_08