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HRID 237586作成日:2026年10月26日

Sodium Carbonate → 6-(4-Amino-3,5-dimethylphenyl)-3-methylpyrimidin-4(3H)-one

https://huagongshe.com/reaction/237586

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6-Chloro-3-methylpyrimidin-4(3H)-oneHCID 4366471—
反応物2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 56737724—
溶媒DimethylformamideHCID 6228—
生成物6-(4-Amino-3,5-dimethylphenyl)-3-methylpyrimidin-4(3H)-oneHCID 86697249—

反応条件

温度65 °C

反応手順

In a microwave vial 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (5.6 g) and 6-chloro-3-methylpyrimidin-4(3H)-one (3 g) are suspended in N,N-dimethylformamide (30 mL) and Na2CO3 (26 mL of a 2M aqueous solution). The mixture is purged for 5 minutes with argon. [1,1′-Bis(diphenylphosphino)-ferrocene]-dichloropalladium dichloromethane complex (508 mg) is added, the vial is sealed and the mixture is stirred at 65° C. for 12 hours. After cooling to room temperature the mixture is Partitioned between water and ethyl acetate. The aqueous phase is extracted twice with ethyl acetate and the combined organic phases are washed with brine and dried (MgSO4). The solvents are evaporated to give the title compound. Yield: 2.6 g; LC (method 11): tR=0.71 min; Mass spectrum (ESI+): m/z=230 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642585B2
出典データセットuspto-grants-2014_02
ORD IDord-c31715c430bd41598881d2f21c3a7fac
出典メモuspto-grants-2014_02