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HRID 383775作成日:2026年10月25日

Toluene → 3-Methoxy-5-[4-[(3-pyridin-3-ylpyrrolidin-1-yl)carbonyl]-3',5'-bis(trifluoromethyl)biphenyl-2-yl]pyridine

https://huagongshe.com/reaction/383775

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Sodium CarbonateHCID 10340—
反応物3-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridineHCID 3866161—
反応物3-(1-{[2-Bromo-3',5'-bis(trifluoromethyl)biphenyl-4-yl]carbonyl}pyrrolidin-3-yl)pyridineHCID 86657753—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒EthanolHCID 702—
生成物3-Methoxy-5-[4-[(3-pyridin-3-ylpyrrolidin-1-yl)carbonyl]-3',5'-bis(trifluoromethyl)biphenyl-2-yl]pyridineHCID 86657752—

反応条件

温度125 °C

反応手順

[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13.7 mg, 0.019 mmol) was added to a solution of 3b (51.0 mg, 0.094 mmol), 3-methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (24.3 mg, 0.103 mmol) and sodium carbonate (94.0 μL, of a 2.0 M aqueous solution, 0.188 mmol) in EtOH:toluene (1.25 mL of an 80:20 mixture, respectively) at rt. The resulting solution was heated to 125° C. in a sealed microwave vial for 12 min. After cooling to rt, the reaction mixture was filtered through a short column of Celite®, eluting with EtOAc. The filtrate was washed with water and brine, dried (sodium sulfate) and concentrated in vacuo. The crude residue was purified by preparative reversed phase HPLC on YMC Pack Pro C18 stationary phase (CH3CN/H2O as eluent, 0.05% TFA as modifier), followed by lyophilization of the purified fractions afforded the title compound 3c. m/z (ES) 572 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367679B2
出典データセットuspto-grants-2013_02
ORD IDord-375568f3d46d434fbe85ed83ce9dcafc
出典メモuspto-grants-2013_02