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HRID 2205734作成日:2026年10月26日

Sodium Carbonate → 2-Chloro-3-methyl-5-(4-(trifluoromethoxy)phenyl)pyridine

https://huagongshe.com/reaction/2205734

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Potassium CarbonateHCID 11430—
反応物1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
反応物2-Chloro-3-methylpyridine-5-boronic acidHCID 17750236—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
溶媒Ammonium ChlorideHCID 25517—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Chloro-3-methyl-5-(4-(trifluoromethoxy)phenyl)pyridineHCID 58118982—

反応手順

To a solution of 1-iodo-4-(trifluoromethoxy)benzene (288 mg, 1.0 mmol) and 6-chloro-5-methylpyridin-3-ylboronic acid (223 mg, 1.3 mmol) in DMF (2 mL) was added K2CO3 (552 mg, 4.0 mmol) and H2O (0.5 mL). The reaction mixture was stirred for 5 min under an atmosphere of dry N2. Pd(PPh3)4 (10 mg, 0.009 mmol) was added, and the resulting mixture was subjected to irradiation at 120° C. for 10 min. Cooled, diluted with EtOAc (20 mL), filtered through a layer of celite, washed with 10% DMF in EtOAc (50 mL), transferred to a separation funnel, organic phase was washed with 2N Na2CO3 (20 mL, 4.00 mmol), H2O (20 mL), 30% aqueous NH4Cl (50 mL) and brine (50 mL), and dried and concentrated. The crude mixture was subjected to preparative HPLC with a gradient MeCN/H2O (5% to 98%) containing 0.1% TFA to afford 2-chloro-3-methyl-5-(4-(trifluoromethoxy)phenyl)pyridine,

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09371329B2
出典データセットuspto-grants-2016_06
ORD IDord-f302e970e2cb4470993d6499e52cba57
出典メモuspto-grants-2016_06