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HRID 216135作成日:2026年10月26日

Cesium carbonate → 4-Chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidine

https://huagongshe.com/reaction/216135

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4,6-Dichloro-2-(methylthio)pyrimidineHCID 80531—
反応物(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-Chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidineHCID 57636137—

反応手順

A mixture of 2-methoxy-5-pyridyl-boronic acid (600 mg, 2.04 mmol, Intermediate (37), prepared according to the procedure described in J. Org. Chem., 67, 7541, 2002), 4,6-dichloro-2-methylsulfanyl-pyrimidine [700 mg, 3.59 mmol, Intermediate (29)], and Cs2CO3 (2.9 g, 8.97 mmol) in ethylene glycol dimethyl ether (8 mL) and water (2 mL) is degassed by bubbling with Argon gas for 5 minutes, and treated with tetrakis(triphenylphosphine)palladium(0) (207 mg, 0.18 mmol) at room temperature. After 3 hours at 85° C., the mixture is diluted with water (50 mL), and extracted twice with EtOAc (50 mL). The extracts are dried over magnesium sulfate, filtered, and concentrated to afford 4-chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidine [1.1 g, Intermediate (38)] as an oil. LCMS: RT=3.72 minutes, MS: 268 (M+H).

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-1da3546174374a378f542f919405334d
出典メモuspto-grants-2012_06