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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74234생성일: 2026년 10월 25일

Phenylacetaldehyde → 5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazole

https://huagongshe.com/reaction/74234

반응식

참여 물질

역할이름HCID투입량
반응물PhenylacetaldehydeHCID 998—
반응물Potassium CarbonateHCID 11430—
반응물Potassium hydroxy sulfiteHCID 23707502—
반응물5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoanilineHCID 67498806—
용매DimethylformamideHCID 6228—
생성물5-(Benzoxazol-2-yl)-2-benzyl-1-(tetrahydropyran-4-yl)benzimidazoleHCID 6749808042%

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 (3 mL) was added phenylacetaldehyde (101 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 (110 mg, 42% yield) as light brown amorphous mass.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829035B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0bbbe93463ce44a8911d4cac7a6abf1f
출처 메모uspto-grants-2014_09