HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Imidazo(4,5-b)pyridine | HCID 67504 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 8-Bromo-6-chloro-2-(4-chlorophenyl)imidazo[1,2-a]pyridine | HCID 14234917 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Hexamethylphosphoramide | HCID 12679 | — |
| Produkt | 6-Chloro-2-(4-chlorophenyl)-8-methoxyimidazo[1,2-a]-pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04847263 |
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| Quelldatensatz | uspto-grants-1989_07 |
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| ORD ID | ord-036eebe4c5f849078205be171443b810 |
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| Quellennotiz | uspto-grants-1989_07 |
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