돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 586374생성일: 2026년 10월 25일

2-(3-fluorophenyl)-1H-imidazole → 6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/586374

반응식

참여 물질

역할이름HCID투입량
반응물2-(3-fluorophenyl)-1H-imidazoleHCID 316816—
반응물Dichloromethane methanolHCID 21226129—
반응물2-Chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridineHCID 22335107—
용매Ethyl AcetateHCID 8857—
용매DimethylacetamideHCID 31374—
생성물6-chloro-2-{[2-(3-fluorophenyl)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridineHCID 22335084—

반응 조건

온도60 °C

반응 단계

Kt-BuO (0.69 mL of 1 M in THF, 0.69 mmol) is added to a solution of 3-fluoro-(1H-imidazol-2-yl)benzene (88 mg, 0.58 mmol) in anhydrous DMA (1 mL). After 15 minutes, 2-chloromethyl-6-chloro-3-(1-propyl)-imidazolo[1,2-a]pyridine (140 mg, 0.58 mmol) is added and the reaction mixture is stirred and heated at 60° C. for 15 minutes. The reaction mixture is diluted with EtOAc (10 mL), washed with water (3 mL), brine (3 mL), dried over Na2SO4, filtered and evaporated at reduced pressure to obtain a yellow solid. Sequential chromatography on silica gel eluting with EtOAc and then 5%MeOH/CH2Cl2 provides 6-chloro-2-{[2-(3-fluoropheny)-1H-imidazol-1-yl]methyl}-3-propylimidazo[1,2-a]pyridine as a cream-colored yellow solid. TLC (10% MeOH/CH2Cl2) Rf=0.35.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06936617B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-8d638e36cfbd4aaab052ecb27541dd34
출처 메모uspto-grants-2005_08