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HRID 2110663作成日:2026年10月27日

Sodium Carbonate → [2-(2-Chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amine

https://huagongshe.com/reaction/2110663

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2-(2-Chloro-6-fluorophenyl)ethan-1-amineHCID 2734094—
反応物4-Chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidineHCID 57636137—
溶媒WaterHCID 962—
溶媒1-MethylpyrrolidineHCID 8454—
生成物[2-(2-Chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amineHCID 1155321094.5%

反応条件

温度175 °C

反応手順

A mixture of 2-(2-chloro-6-fluoro-phenyl)-ethylamine [1.02 g, 5.88 mmol, Intermediate (23)], Na2CO3 (1.65 g, 19.6 mmol), and 4-chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidine [1.05 g, 3.92 mmol, Intermediate (38)] in N-methyl pyrrolidine (10 mL), is heated to 175° C. for 3 hours. The reaction mixture is diluted with water, and extracted with ethyl acetate. The extracts are washed with water, dried over magnesium sulfate, filtered, and concentrated. The residue is subjected to short-path chromatography on silica gel eluting with EtOAc to afford [2-(2-chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amine [1.5 g, Example 30]. LCMS: RT=3.37 minutes, MS: 405 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07517889B2
出典データセットuspto-grants-2009_04
ORD IDord-07b927087b194c79b4bd062a3d27ea5f
出典メモuspto-grants-2009_04