戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 595156作成日:2026年10月25日

Sodium Carbonate → N-(3-(1-(cyclohex-2-en-1-yl)-1H-pyrazol-4-yl)-5-methylphenyl)-4-(difluoromethyl)pyrimidin-2-amine

https://huagongshe.com/reaction/595156

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N-(3-bromo-5-methylphenyl)-4-(difluoromethyl)pyrimidin-2-amineHCID 67249363—
反応物1-Cyclohex-2-enyl-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazoleHCID 122201640—
溶媒1,4-DioxaneHCID 31275—
生成物N-(3-(1-(cyclohex-2-en-1-yl)-1H-pyrazol-4-yl)-5-methylphenyl)-4-(difluoromethyl)pyrimidin-2-amineHCID 118208720—

反応条件

温度110 °C

反応手順

1-(Cyclohex-2-en-1-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (436 mg, 1.59 mmol), sodium carbonate (337 mg, 3.18 mmol), and 1,1′-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (130 mg, 0.159 mmol) were added to a solution of N-(3-bromo-5-methylphenyl)-4-(difluoromethyl)pyrimidin-2-amine (500 mg, 1.59 mmol) in dioxane (7.5 mL). The mixture was purged with nitrogen for 5 minutes and stirred at 110° C. for 18 h. The mixture was allowed to cool to room temperature, diluted with water (30 mL) and extracted with ethyl acetate (3×50 mL). The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (0-50% EtOAc/hexane) to afford N-(3-(1-(cyclohex-2-en-1-yl)-1H-pyrazol-4-yl)-5-methylphenyl)-4-(difluoromethyl)pyrimidin-2-amine ESI calc'd. for C21H22F2N5 [M+H]+ 382. found 382.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09242984B2
出典データセットuspto-grants-2016_01
ORD IDord-befba7af195444ff99153f701a9154da
出典メモuspto-grants-2016_01