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HRID 231533Erstellt: 26. Oktober 2026

Imidazo(4,5-b)pyridine → 6-Chloro-2-(4-chlorophenyl)-8-methoxyimidazo[1,2-a]-pyridine

https://huagongshe.com/reaction/231533

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktImidazo(4,5-b)pyridineHCID 67504—
EduktSodiumHCID 5360545—
EduktSodium MethoxideHCID 10942334—
Edukt8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelHexamethylphosphoramideHCID 12679—
Produkt6-Chloro-2-(4-chlorophenyl)-8-methoxyimidazo[1,2-a]-pyridineHCID 14234923—

Reaktionsschritte

10 g (29.4 mmol) of 8-bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine, the preparation of which compound is described in the patent application filed this day entitled: Derives d'imidazopyridines, leur preparation et leur application en therapeutique (Imidazopyridine derivatives, their preparation and their application in therapy) by the Applicant, dissolved in 60 ml of hexamethylphosphorotriamide, are added to a solution of sodium methylate prepared using 2.03 g of sodium and 15 ml of methanol, the reaction mixture is brought to 60° C. for 2 h 30 min., water is added, the mixture is extracted with CH2Cl2, the organic phase is washed with water, dried over MgSO4 and filtered, and the filtrate is concentrated under reduced pressure. The evaporation residue is recrystallized in an ethyl acetate/hexane mixture. M.p. 150°-151° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04847263
Quelldatensatzuspto-grants-1989_07
ORD IDord-036eebe4c5f849078205be171443b810
Quellennotizuspto-grants-1989_07