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HRID 278088作成日:2026年10月27日

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

https://huagongshe.com/reaction/278088

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物Butyryl chlorideHCID 8855—
反応物(E)-Methyl 4-(2-(dimethylamino)vinyl)-3-nitrobenzoateHCID 894337—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(1-dimethylaminomethylene-2-oxopentyl)-3-nitrobenzoateHCID 54551046—

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358992B1
出典データセットuspto-grants-2002_03
ORD IDord-31ba064805a246c6b756045b3250a457
出典メモuspto-grants-2002_03