돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253460생성일: 2026년 10월 25일

Dimethylformamide → 4-(1H-benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehyde

https://huagongshe.com/reaction/253460

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-Fluoro-4-hydroxy-5-methoxybenzaldehydeHCID 598155—
반응물4-(1H-benzoimidazol-2-ylmethoxy)-5-chloro-2-fluoro-benzaldehydeHCID 59803854—
용매WaterHCID 962—
생성물4-(1H-benzimidazol-2-ylmethoxy)-2-fluoro-5-methoxy-benzaldehydeHCID 5808602045.6%

반응 단계

2-Fluoro-4-hydroxy-5-methoxy-benzaldehyde (39, 0.290 g, 1.7 mmol, prepared as described in Scheme 12 of Example 15) was dissolved in N,N-dimethylformamide (20 mL, 200 mmol). Sodium hydride (60% dispersion in oil, 0.852 g, 2.13 mmol) was added to the solution and after the mixture was stirred for 20 minutes at room temperature, 2-chloromethyl-1H-benzoimidazole (106, 0.28 g, 1.7 mmol) was added to the reaction. The obtained mixture was heated to 80° C. and stirred overnight. After cooling to room temperature, the reaction was poured into water and extracted with ethyl acetate. The organic portion was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated and purified by silica gel column chromatography eluting with a gradient of ethyl acetate (40 to 100%) in hexane to give the desired compound (142, 0.233 g, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872018B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-26eea312addc4aae9419fdc5fcd4839b
출처 메모uspto-grants-2011_01