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HRID 1108702생성일: 2026년 10월 25일

Pyridine → Methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoate

https://huagongshe.com/reaction/1108702

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Butyryl chlorideHCID 8855—
반응물(E)-Methyl 4-(2-(dimethylamino)vinyl)-3-nitrobenzoateHCID 894337—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoateHCID 54551046—

반응 조건

온도50 °C

반응 단계

To a stirred mixture of methyl (E)-4-[2-(dimethylamino)vinyl]-3-nitrobenzoate (500 mg), which was prepared by the method of Brown et al. described in Journal of Medicinal Chemistry, vol. 35, page 2419 (1992), and pyridine (0.16 ml) in tetrahydrofuran (3 ml) was added butyryl chloride (0.21 ml) at 20° C. The reaction mixture was stirred at 40° C. for 24 hours and 50° C. for 4 hours. After cooled to 20° C., the reaction mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water and brine, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:1) to give methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoate (426 mg) as colorless amorphous.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06069156
출처 데이터셋uspto-grants-2000_05
ORD IDord-1fcbf5fece15453f9a552fa4c964373e
출처 메모uspto-grants-2000_05