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HRID 231533생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/231533

반응식

참여 물질

역할이름HCID투입량
반응물Imidazo(4,5-b)pyridineHCID 67504—
반응물SodiumHCID 5360545—
반응물Sodium MethoxideHCID 10942334—
반응물8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridineHCID 14234917—
용매MethanolHCID 887—
용매WaterHCID 962—
용매HexamethylphosphoramideHCID 12679—
생성물6-Chloro-2-(4-chlorophenyl)-8-methoxyimidazo[1,2-a]-pyridineHCID 14234923—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847263
출처 데이터셋uspto-grants-1989_07
ORD IDord-036eebe4c5f849078205be171443b810
출처 메모uspto-grants-1989_07