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HRID 222941作成日:2026年10月26日

Biphenyl → 4-(5-amino-2-methylphenyl)-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one

https://huagongshe.com/reaction/222941

反応式

関与物質

役割名称HCID仕込み量
反応物BiphenylHCID 7095—
反応物TriethylamineHCID 8471—
反応物3-Iodo-p-toluidineHCID 118889—
反応物PinacolboraneHCID 6364989—
反応物4-Chloro-2-methylsulfanyl-8-(2,6-difluorophenyl)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11951513—
反応物Barium hydroxide, octahydrateHCID 17749109—
触媒palladium(II) acetateHCID 167845—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物4-(5-amino-2-methylphenyl)-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 5921267980.3%

反応条件

温度80 °C

反応手順

To a solution of 3-iodo-4-methylaniline (110.0 mg, 0.47 mmol) in dioxane (1.0 mL) was added (under argon) triethylamine (0.26 mL, 1.86 mmol), palladium diacetate (5.2 mg, 0.023 mmol), 2-(dicyclophexyl phosphino) biphenyl (33.0 mg, 0.093 mmol), and pinacolborane (0.20 mL, 1.40 mmol). The mixture was stirred at about 80° C. for about 1 hour, cooled to room temperature (rt), and added with water (0.2 mL), barium hydroxide octahydrate (440.0 mg, 1.40 mmol) and 4-chloro-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (180.0 mg, 0.47 mmol). The mixture was heated at about 100° C. under stirring for about 1 hour, cooled to room temperature, filtered through celite, and diluted with brine (5.0 mL). The mixture was then extracted with CH2Cl2 (3×10 mL). The combined organic phases were dried over Na2SO4, filtered, and concentrated. Purification via the CombiFlash system then afforded the title compound (155.0 mg, 75%): LC-MS m/z 411 (M+H)+, 2.60 min (ret. time).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207176B2
出典データセットuspto-grants-2012_06
ORD IDord-b35000c270a04566af2d6062f5ff9a44
出典メモuspto-grants-2012_06