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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1181318생성일: 2026년 10월 27일

Ethyl Acetate → Ethyl 1-cyclohexyl-2-{4-[(E)-2-phenylvinyl]phenyl}-benzimidazole-5-carboxylate

https://huagongshe.com/reaction/1181318

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물BenzofuroxanHCID 68075—
반응물Ferrostatin-1HCID 4068248—
반응물4-Formyl-trans-stilbeneHCID 5375876—
용매MethanolHCID 887—
용매AcetonitrileHCID 6342—
생성물Ethyl 1-cyclohexyl-2-{4-[(E)-2-phenylvinyl]phenyl}-benzimidazole-5-carboxylateHCID 1011485563%

반응 단계

Ethyl 3-amino-4-cyclohexylaminobenzoate (500 mg) obtained in Example 1, Step 3, was dissolved in methyl alcohol (6 ml) and trans-4-stilbenecarbaldehyde (397 mg) was added under ice-cooling. The mixture was stirred overnight at room temperature. The reaction mixture was ice-cooled and benzofuroxan (259 mg) dissolved in acetonitrile (2 ml) was added. The mixture was stirred for 7 hr at 50° C., The reaction mixture was ice-cooled. After 1N sodium-hydroxide was added, ethyl acetate was added and the mixture was extracted. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (developing solvent, n-hexane:ethyl acetate=4:1) to give the title compound (540 mg, yield 63%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07285551B2
출처 데이터셋uspto-grants-2007_10
ORD IDord-4fab5b69516e43e587c8bb1a1e14fa77
출처 메모uspto-grants-2007_10