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HRID 465997作成日:2026年10月26日

Pyridazine → 3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/465997

反応式

関与物質

役割名称HCID仕込み量
反応物PyridazineHCID 9259—
反応物Ethyl chloroformateHCID 10928—
反応物2-Phenylpyrazolo[1,5-a]pyridineHCID 15620342—
溶媒DichloromethaneHCID 6344—
生成物3-(1-Ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridineHCID 1179186053.4%

反応条件

温度10 °C

反応手順

Ethyl chloroformate (3.38 g) was added dropwise with stirring to a solution of 2-phenylpyrazolo[1,5-a]pyridine (2.54 g) and pyridazine (5.00 g) in methylene chloride (5.0 ml) at 10° C. After being stirred at 10° C. for 1 hour and then at room temperature for 2 hours, the reaction mixture was poured onto ice-water (100 ml), and extracted with ethyl acetate. The combined extracts were washed with saturated sodium chloride aqueous solution (100 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (150 g) with a mixture of chloroform and n-hexane (1:1) as an eluant. The fractions containing main-product [compound (A)] were combined and evaporated in vacuo to give 3-(1-ethoxycarbonyl-1,4-dihydropyridazin-4-yl)-2-phenylpyrazolo[1,5-a]pyridine (2.42 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05155114
出典データセットuspto-grants-1992_10
ORD IDord-c7262b43437944ed8a03a8289694a8d5
出典メモuspto-grants-1992_10