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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74236생성일: 2026년 10월 23일

3-Furaldehyde → 5-(Benzoxazol-2-yl)-2-(furan-3-yl)-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/ko/reaction/74236

반응식

참여 물질

역할이름HCID투입량
반응물3-FuraldehydeHCID 10351—
반응물Potassium CarbonateHCID 11430—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
용매DimethylformamideHCID 6228—
생성물5-(Benzoxazol-2-yl)-2-(furan-3-yl)-1-(tetrahydropyran-4-yl)benzimidazoleHCID 4982145969%

반응 단계

To a solution of 5-(benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (200 mg, 0.646 mmol) in dimethylformamide (2 mL) was added 3-furaldehyde (80.7 mg, 0.840 mmol) and oxone (258 mg, 0.420 mmol), and this was stirred at room temperature for 3 hours. After the reaction was complete, aqueous potassium carbonate solution was added, this was filtered and washed with water. The crystals obtained were purified by silica gel column chromatography to yield the title compound (171 mg, 69% yield) as pale yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-3654201990e44b268913e761ca02e6fd
출처 메모uspto-grants-2014_09