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HRID 521893作成日:2026年10月25日

Tris(1,1-dimethylethyl)phosphine → Methyl 2-(2,6-difluoro-4-methoxy-phenyl)thiazole-4-carboxylate

https://huagongshe.com/reaction/521893

反応式

関与物質

役割名称HCID仕込み量
反応物Tris(1,1-dimethylethyl)phosphineHCID 83681—
反応物Potassium FluorideHCID 522689—
反応物Methyl 2-bromothiazole-4-carboxylateHCID 2763213—
反応物2,6-Difluoro-4-methoxybenzeneboronic acidHCID 16217424—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-(2,6-difluoro-4-methoxy-phenyl)thiazole-4-carboxylateHCID 8671385074%

反応条件

温度100 °C

反応手順

To a solution of methyl 2-bromothiazole-4-carboxylate (3.27 mmol, 741 mg) in tetrahydrofuran (15 mL) and water (1.5 mL) was added 2,6-difluoro-4-methoxyphenylboronic acid (1.8 equiv., 5.88 mmol, 1160 mg) and potassium fluoride (3.3 equiv., 10.8 mmol, 627 mg). The mixture was degassed with nitrogen, then tris(dibenzylideneacetone)dipalladium(0) (0.2 equiv., 0.654 mmol, 617 mg) and tri-tert-butylphosphine (1.0 M in toluene; 0.4 equiv., 1.31 mmol, 1.3 mL) were added and the reaction mixture was heated under microwave at 100° C. for 30 minutes. The reaction mixture was concentrated and the residue was purified on silica eluted with 0 to 50% EtOAc in heptane to afford methyl 2-(2,6-difluoro-4-methoxy-phenyl)thiazole-4-carboxylate (2.40 mmol, 685 mg, 74% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328106B2
出典データセットuspto-grants-2016_05
ORD IDord-0c202543724941d6853a27b6150abbbb
出典メモuspto-grants-2016_05