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HRID 44201作成日:2026年10月25日

Sodium Carbonate → 4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/44201

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1,4-DioxaneHCID 31275—
反応物4-Chloro-5-methoxy-2-methyl-2,3-dihydropyridazin-3-oneHCID 2774938—
反応物2-Ethylphenylboronic Acid (contains varying amounts of Anhydride)HCID 4100862—
触媒Tetrabutylammonium BromideHCID 74236—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
生成物4-(2-ethylphenyl)-5-methoxy-2-methyl-3(2H)-pyridazinoneHCID 5743731792%

反応手順

To a mixture of 2.516 g of 4-chloro-5-methoxy-2-methyl-3 (2H)-pyridazinone, 2.575 g of 2-ethylphenylboronic acid and 3.333 g of sodium carbonate were added 30 mL of 1,4-dioxane and 20 mL of water. To the mixture were added 2.417 g of tetrabutylammonium bromide and 0.657 g of tetrakis(triphenylphosphine)palladium, and then under a nitrogen atmosphere, the resulting mixture was stirred and heated under reflux for 17 hours. After cooling, 50 mL of water was added to the reaction mixture, which was extracted with 100 mL of ethyl acetate and then 30 mL of ethyl acetate. The extracts were combined, washed with a saturated sodium chloride aqueous solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off. The solid obtained was washed with a mixed solvent of ethyl acetate and hexane (1:2) to yield 3.238 g of the title compound as yellow crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541414B2
出典データセットuspto-grants-2013_09
ORD IDord-2b623f1378b44c2bbd7832ddf0ef79d5
出典メモuspto-grants-2013_09