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HRID 59153作成日:2026年10月25日

2-(Dicyclohexylphosphino)biphenyl → N2-(3-Methoxy-4-(6-methylpyridazin-4-yl)phenyl)-N4-methyl-6-((2,2,2-trifluoroethoxy)-methyl)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/59153

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Dicyclohexylphosphino)biphenylHCID 2734216—
反応物CesiumHCID 5354618—
反応物3-Methoxy-4-(6-methylpyridazin-4-yl)anilineHCID 66859066—
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N2-(3-Methoxy-4-(6-methylpyridazin-4-yl)phenyl)-N4-methyl-6-((2,2,2-trifluoroethoxy)-methyl)pyrimidine-2,4-diamineHCID 86344800—

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 (50 mg, 0.20 mmol), 3-methoxy-4-(6-methylpyridazin-4-yl)aniline (42 mg, 0.20 mmol), cesium rbonate (127 mg, 0.39 mmol), palladium (II) acetate (7 mg, 0.03 mmol) and 2-(dicyclohexylphosphino)-biphenyl (10 mg, 0.03 mmol) in dioxane (2 mL) was heated under argon at 120° C. for 90 minutes in a microwave reactor. 2-Chloro-N-methyl-6-((2,2,2-trifluoroethoxy)methyl)pyrimidin-4-amine (72 mg, 0.28 mmol, 1.4 eq), palladium(II) acetate (7 mg) and 2-(dicyclohexylphosphino)biphenyl (10 mg) was added and the mixture was heated at 120° C. for 90 minutes in a microwave reactor. The mixture was filtered through a short silica gel plug which was washed with 10% solution of methanol in ethyl acetate (75 mL). The eluate was concentrated in vacuum and the residue was purified by preparative to give the title compound as a solid, 22 mg (26%).

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-766617a20112464390c873db4aff3d00
出典メモuspto-grants-2016_09