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HRID 28538作成日:2026年10月24日

Sodium Carbonate → 4-Chloro-6-(5-chloro-2-methylphenyl)pyrimidin-2-yl-amine

https://huagongshe.com/ja/reaction/28538

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TriphenylphosphineHCID 11776—
反応物2-Amino-4,6-dichloropyrimidineHCID 65522—
反応物(5-Chloro-2-methylphenyl)boronic acidHCID 2773336—
触媒palladium(II) acetateHCID 167845—
溶媒AcetoneHCID 180—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-Chloro-6-(5-chloro-2-methylphenyl)pyrimidin-2-yl-amineHCID 8600434740.3%

反応手順

To a mixture of 4,6-dichloro-2-amino-pyrimidine (0.481 g, 2.93 mmol), 5-chloro-2-methyl-phenyl boronic acid (0.5 g, 2.93 mmol), palladium (II) acetate (0.1 g, 0.44 mmol), and triphenylphosphine (0.23 g, 0.88 mmol) was added a solution of sodium carbonate (1.5 g, 14.6 mmol) in water (5.0 ml) followed by glyme (20 ml). The mixture was stirred under an argon atmosphere for 16 hours. After addition of acetone (15 ml), the mixture was filtered through a pad of celite under suction and the filtrate was concentrated under vacuum. The residual solid was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:9). After concentration under reduced pressure, the solid was dissolved in methanol and a solution of hydrogen chloride in dioxane (4.0 M, 5 ml) was added. After concentration under vacuum, the solid was treated with ethyl acetate (5 ml) and stirred for one hour. Filtration provided the hydrochloride salt of 4-chloro-6-(5-chloro-2-methyl-phenyl) pyrimidin-2-yl-amine (0.30 g, 35% yield) as a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419984B2
出典データセットuspto-grants-2008_09
ORD IDord-52d60904d655427e82e02ae00f5b1749
出典メモuspto-grants-2008_09