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HRID 231533作成日:2026年10月27日

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

https://huagongshe.com/reaction/231533

反応式

関与物質

役割名称HCID仕込み量
反応物Imidazo(4,5-b)pyridineHCID 67504—
反応物SodiumHCID 5360545—
反応物Sodium MethoxideHCID 10942334—
反応物8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒HexamethylphosphoramideHCID 12679—
生成物6-Chloro-2-(4-chlorophenyl)-8-methoxyimidazo[1,2-a]-pyridineHCID 14234923—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04847263
出典データセットuspto-grants-1989_07
ORD IDord-036eebe4c5f849078205be171443b810
出典メモuspto-grants-1989_07