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HRID 252013作成日:2026年10月25日

Hydrochloric Acid → Ethyl 2-(3-Chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylate

https://huagongshe.com/reaction/252013

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物3-Chloro-2-hydrazinylpyridineHCID 556100—
反応物Sodium ethoxideHCID 2723922—
反応物Diethyl MaleateHCID 5271566—
溶媒Acetic AcidHCID 176—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物Ethyl 2-(3-Chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylateHCID 22280352—

反応条件

温度65 °C

反応手順

To a mixture of 20 g of 3-chloro-2-hydrazinopyridine, 56 ml of sodium ethoxide (a 21% solution in ethanol) and 75 ml of ethanol was added dropwise 27 ml of diethyl maleate. The resulting mixture was heated to reflux for 10 minutes. The reaction mixture was allowed to cool to 65° C., and 15 ml of acetic acid was poured into the mixture. The reaction mixture was allowed to cool to room temperature. After 190 ml of water was poured into the reaction mixture, the mixture was adjusted to pH 2 by an addition of 6N hydrochloric acid and then extracted with methyl tert-butyl ether three times. The organic layers were combined, washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. Diethyl ether was added to the resulting residue, and a solid was collected by filtration to obtain 4.28 g of ethyl 2-(3-chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylate of the formula:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867949B2
出典データセットuspto-grants-2011_01
ORD IDord-14f852d1d4f649db8f9598f649336091
出典メモuspto-grants-2011_01