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HRID 1845538作成日:2026年10月26日

Potassium Carbonate → methyl 5-chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylate

https://huagongshe.com/reaction/1845538

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 4912908—
反応物Methyl 4-Bromo-5-chloro-2-furoateHCID 12239445—
触媒HCID 178418851HCID 178418851—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物methyl 5-chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylateHCID 5782677055.1%

反応手順

A solution of methyl 4-bromo-5-chloro-2-furancarboxylate (1.1 g, 4.59 mmol), 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (1.05 g, 5.05 mmol) [prepared according to Preparation 7], potassium carbonate (3.17 g, 22.97 mmol) and bis(tri-t-butylphosphine)palladium(0) (0.117 g, 0.23 mmol) in 1,4-dioxane (19.14 ml) and water (3.83 ml) was stirred at 80° C. in a sealed tube for 1 h. The reaction mixture was partitioned between H2O-DCM and the aqueous phase was washed several times with DCM. The combined organic fractions were dried over Na2SO4, concentrated and purified via column chromatography (silica, 4-25% EtOAc in hexanes) yielding methyl 5-chloro-4-(1-methyl-1H-pyrazol-5-yl)-2-furancarboxylate (800 mg, 2.53 mmol, 55% yield) as a yellow oil: LCMS m/e ES 240, 242 (M, M+2)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08946278B2
出典データセットuspto-grants-2015_02
ORD IDord-36a0034e0af645b197d7640e1ba9824a
出典メモuspto-grants-2015_02