戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 216151作成日:2026年10月23日

Isopropanol → 4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidine

https://huagongshe.com/ja/reaction/216151

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Cesium carbonateHCID 10796—
反応物4,6-Dichloro-2-(methylthio)pyrimidineHCID 80531—
反応物3,4-Dimethoxyphenylboronic acidHCID 2734702—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidineHCID 5763614683.6%

反応条件

温度100 °C

反応手順

Argon is bubbled through a mixture of 4,6-dichloro-2-(methylthio)pyrimidine [4.98 g, 25.55 mmol, Intermediate (29)], 3,4-dimethoxyphenylboronic acid [3.874 g, 21.29 mmol, Intermediate (32)], and Cs2CO3 (17.34 g, 53.23 mmol) in ethylene glycol dimethyl ether (56 mL) and water (14 mL), for a period of 15 minutes. To this mixture is added tetrakis(triphenylphosphine)palladium (0) (1.22 g, 1.06 mmol) the reaction vessel is heated to 100° C. After stirring overnight the mixture is diluted with water (250 mL) and extracted three times with EtOAc (100 mL). The organic extracts are combined, washed with brine (100 mL), and dried over magnesium sulfate. The mixture is filtered and concentrated to provide a solid that is dissolved in boiling isopropyl alcohol (40 mL) and allowed to cool to ambient temperature. After standing for 24 hours the solid is collected by filtration, washed with cold isopropyl alcohol and dried under high vacuum to afford 4-chloro-6-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-pyrimidine [5.28 g, 83.5%, Intermediate (48)].

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08193183B2
出典データセットuspto-grants-2012_06
ORD IDord-ebeec63bcd6a4bdfb9ce05b0a1a3d940
出典メモuspto-grants-2012_06