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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74191생성일: 2026년 10월 23일

3-Pyridinecarboxaldehyde → 5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/ko/reaction/74191

반응식

참여 물질

역할이름HCID투입량
반응물3-PyridinecarboxaldehydeHCID 10371—
반응물Potassium CarbonateHCID 11430—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749789349.5%

반응 단계

5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (0.15 g, 0.484 mmol) was dissolved in DMF (3 mL) and water (0.1 mL), 3-pyridinecarboxaldehyde (0.06 g, 0.561 mmol) was added followed by oxone (0.19 g, 0.310 mmol), and this was stirred at room temperature for 2.5 hours. Aqueous potassium carbonate solution (0.09 g/15 mL) was added to the reaction solution. This was extracted with chloroform, washed with water, and after drying over magnesium sulfate, this was concentrated and purified by silica gel column chromatography. The crystals obtained were washed with hexane and a small amount of ethyl acetate, and dried to yield the title compound (95.0 mg, 49.5% yield) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-897d73089fb64b02b603065e4363a006
출처 메모uspto-grants-2014_09