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HRID 59133作成日:2026年10月25日

Cesium carbonate → N4-Methyl-N2-(4-(4-methyl-1H-imidazol-1-yl)phenyl)-6-((2,2,2-trifluoroethoxy)methyl)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/59133

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物2-(Dicyclohexylphosphino)biphenylHCID 2734216—
反応物4-(4-Methyl-1h-imidazol-1-yl)benzenamineHCID 16005170—
反応物2-Chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amineHCID 117821210—
触媒palladium(II) acetateHCID 167845—
溶媒1,4-DioxaneHCID 31275—
生成物N4-Methyl-N2-(4-(4-methyl-1H-imidazol-1-yl)phenyl)-6-((2,2,2-trifluoroethoxy)methyl)-pyrimidine-2,4-diamineHCID 8634443140.2%

反応条件

温度120 °C

反応手順

A mixture of 2-chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amine (85 mg, 0.33 mmol), 4-(4-methyl-1H-imidazol-1-yl)aniline (100 mg, 0.58 mmol), cesium carbonate (217 mg, 0.67 mmol), palladium(II) acetate (11 mg, 0.05 mmol) and 2-(dicyclohexylphosphino)-biphenyl (17 mg, 0.05 mmol) in dioxane (3 mL) was heated in a microwave reactor under notrogen atmosphere at 120° C. for 90 min. The reaction mixture was filtered through a pad of diatomeous earth which was eluted with MeOH. The mixture was partitioned between EtOAc and sodium hydroxide (aq, 1 M). The organic phase was separated, dried over sodium sulfate and concentrated in vacuum. The residue was purified by preparative HPLC to give the title compound as a solid 52 mg, (40%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09439904B2
出典データセットuspto-grants-2016_09
ORD IDord-5b10546332b64f55a15b362357df6f61
出典メモuspto-grants-2016_09