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HRID 42710作成日:2026年10月26日

Sodium Carbonate → 2-[5-(Dimethylamino)-2-methyl-3-oxo-2,3-dihydropyridazin-4-yl]benzaldehyde

https://huagongshe.com/reaction/42710

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物2-Formylphenylboronic acidHCID 292189—
反応物4-Chloro-5-(dimethylamino)-2-methylpyridazin-3(2H)-oneHCID 13410294—
反応物Chloroform acetoneHCID 15930782—
触媒HCID 178418397HCID 178418397—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物2-[5-(Dimethylamino)-2-methyl-3-oxo-2,3-dihydropyridazin-4-yl]benzaldehydeHCID 58484360—

反応手順

4-Chloro-5-(dimethylamino)-2-methylpyridazin-3(2H)-one (50.00 mmol) was dissolved in dimethoxyethane (155 ml), and Pd(PPh3)4 (1.60 g, 1.38 mmol) was added under argon. After stirring at room temperature for 10 min, 2-formylbenzeneboronic acid (10.50 g, 70.00 mmol) and 2M Na2CO3 solution (49.5 ml) were added. Subsequently, the reaction mixture was refluxed (oil bath temperature: 110° C.) for 15 h. The reaction was followed by TLC (eluent: chloroform:acetone (9:1)). Upon cooling the reaction mixture was poured onto ice (375 g), filtered over Celite and washed with chloroform (130 ml). The two layers were separated and the aqueous phase was extracted with chloroform (3×380 ml). The combined organic layers were washed with water (1×100 ml), dried over MgSO4, filtered and purified by flash column chromatography with a mixture of diisopropyl ether and acetone (8:1) as the eluent and crystallized from a mixture of ethyl acetate and hexane (2.3:1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536210B2
出典データセットuspto-grants-2013_09
ORD IDord-aeffc808ff7e4f3fb6110e79463d53f0
出典メモuspto-grants-2013_09