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HRID 219206作成日:2026年10月27日

Potassium Phosphate, Tribasic → 5-(3,5-Difluorophenyl)-2,3-difluoropyridine

https://huagongshe.com/reaction/219206

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物(3,5-Difluorophenyl)boronic acidHCID 2734338—
反応物5-Chloro-2,3-difluoropyridineHCID 2783248—
反応物2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenylHCID 11155794—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物5-(3,5-Difluorophenyl)-2,3-difluoropyridineHCID 67502711—

反応条件

温度100 °C

反応手順

A mixture of palladium (II) acetate (0.0375 g, 0.167 mmol), potassium phosphate (2.13 g, 10.0 mmol), 3,5-difluorophenylboronic acid (1.58 g, 10.0 mmol), X-Phos (0.159 g, 0.334 mmol) and 5-chloro-2,3-difluoropyridine (0.347 ml, 3.34 mmol) was diluted with 1,4-dioxane (0.1M, 33.4 mL) and water (0.3M, 11.0 mL) and was heated under nitrogen at 100° C. for 45 minutes. The reaction was concentrated in vacuo. The concentrated material was triturated with water, filtered and rinsed with MeCN. The crude solid was taken up in dichloromethane and filtered over a plug of Celite to eliminate residual palladium. The material was dissolved in minimal DCM, and purified via MPLC (eluting with 0-10% EtOAc in hexanes) to yield 5-(3,5-difluorophenyl)-2,3-difluoropyridine. The material was converted to the hydrazine in a method similar to that in the synthesis of (S)-6-(1-(8-fluoro-6-(3-methylisothiazol-5-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)ethyl)quinoline. The following compounds were prepared using a similar method as 1-(5-(3,5-difluorophenyl)-3-fluoropyridin-2-yl)hydrazine:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08198448B2
出典データセットuspto-grants-2012_06
ORD IDord-09341cb852dc4283a08cb502a2f9bc69
出典メモuspto-grants-2012_06