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HRID 711241作成日:2026年10月26日

Potassium Phosphate, Tribasic → (2'-(Trifluoromethyl)-2,4'-bipyridin-5-yl)methanamine

https://huagongshe.com/reaction/711241

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5-(Aminomethyl)-2-chloropyridineHCID 7020927—
反応物2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
反応物2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
触媒palladium(II) acetateHCID 167845—
溶媒(+-)-2-ButanolHCID 6568—
生成物(2'-(Trifluoromethyl)-2,4'-bipyridin-5-yl)methanamineHCID 67208623—

反応条件

温度100 °C

反応手順

To a flask containing (6-chloropyridin-3-yl)methanamine 33-2 (375 mg, 2.63 mmol), 2-(trifluoromethyl)pyridin-4-ylboronic acid 33-1 (500 mg, 2.63 mmol), Pd(OAc)2 (34 mg, 0.15 mmol), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (S-Phos) (124 mg, 0.30 mmol) and potassium phosphate (1.90 g, 9.00 mmol) under argon was added 2-butanol (4 mL). The mixture was stirred at 100° C. for 10 hours. After cooling to room temperature, the mixture was filtered through celite cake. The filtrate was diluted with ethyl acetate, washed with H2O and brine, dried over Na2SO4, and concentrated to dryness by rotary evaporation. The crude product was purified by silica gel flash chromatography, eluted with 5% methanol containing ˜7N ammonia in dichloromethane to give (2′-(trifluoromethyl)-2,4′-bipyridin-5-yl)methanamine 33-3 as a yellow solid. MS m/z 254.1 (M+1)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181235B2
出典データセットuspto-grants-2015_11
ORD IDord-3bcf7431285b4be586bd389a0b629ac8
出典メモuspto-grants-2015_11