돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 80244생성일: 2026년 10월 25일

Ethyl Acetate → 6-Bromo-3-[[2-(trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/80244

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Sodium HydroxideHCID 14798—
반응물6-Bromo-4H-imidazo[4,5-b]pyridineHCID 911578—
반응물2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
촉매Benzyl triethylammonium chlorideHCID 66133—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물6-Bromo-3-[[2-(trimethylsilyl)ethoxy]methyl]-3H-imidazo[4,5-b]pyridineHCID 1935828814.4%

반응 단계

(2-Chloromethoxy-ethyl)-trimethyl-silane (508.6 mg, 3.0456 mmol), catalytic amount of benzyl triethyl-ammonium chloride and NaOH (203.04 mg, 5.076 mmol) were added to a solution of 6-bromo-3H-imidazo[4,5-b]pyridine (500 mg, 2.538 mmol) in DCM (10 mL) at 0° C. The resulting mixture was stirred room temperature for 6 hours. The reaction was monitored by TLC (80% ethylacetate in hexane). The reaction mixture was partitioned between DCM and water. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (20% ethylacetate in hexane) afforded 120 mg of the product (14.4% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE045173E1
출처 데이터셋uspto-grants-2014_09
ORD IDord-486874dd47bb489285c1af4af84829f7
출처 메모uspto-grants-2014_09