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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2110663Erstellt: 26. Oktober 2026

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-(2-Chloro-6-fluorophenyl)ethan-1-amineHCID 2734094—
Edukt4-Chloro-6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidineHCID 57636137—
LösungsmittelWaterHCID 962—
Lösungsmittel1-MethylpyrrolidineHCID 8454—
Produkt[2-(2-Chloro-6-fluoro-phenyl)-ethyl]-[6-(6-methoxy-pyridin-3-yl)-2-methylsulfanyl-pyrimidin-4-yl]-amineHCID 1155321094,5%

Reaktionsbedingungen

Temperatur175 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07517889B2
Quelldatensatzuspto-grants-2009_04
ORD IDord-07b927087b194c79b4bd062a3d27ea5f
Quellennotizuspto-grants-2009_04