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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 475721Erstellt: 24. Oktober 2026

Ammonia → 6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amine

https://huagongshe.com/de/reaction/475721

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktMethanolHCID 887—
Edukt6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridineHCID 57609300—
LösungsmittelEthylene GlycolHCID 174—
LösungsmittelWaterHCID 962—
Produkt6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amineHCID 53402967100%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine (1.000 g, 3.73 mmol) and cuprous oxide (0.053 g, 0.373 mmol) in 8.3 mL of ethylene glycol was added a 7 N solution of ammonia in methanol (7.99 mL, 55.9 mmol). The reaction mixture was heated in a high-pressure vessel at 100° C. overnight. Upon cooling to room temperature, the reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layers were dried over anhydrous magnesium sulfate and filtered. The solvent was removed in vacuum to give 6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-amine (762.0 mg, 3.73 mmol, 100% yield) as brown semisold. LC-MS (M+H)+=205.10. 1H NMR (500 MHz, CDCl3) δ ppm 7.53 (1H, s), 7.26 (1H, d, J=8.2 Hz), 6.78 (1H, s), 6.07 (1H, d, J=8.2 Hz), 3.86 (3H, s.), 2.25 (3H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637525B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-2bf927a7ae0046eca44869718d36c643
Quellennotizuspto-grants-2014_01