HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4297Erstellt: 25. Oktober 2026
Dimethylamine → 8-(2-Chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/4297
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylamine | HCID 674 | — |
| Edukt | Formaldehyde | HCID 712 | — |
| Edukt | 8-(2-Chlorobenzyloxy)-2-methylimidazo[1,2-a]pyridine | HCID 13825932 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 8-(2-Chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridine | HCID 13825936 | 85,4% |
Reaktionsschritte
To a solution of 37% aqueous formaldehyde (2.38 g) in acetic acid (38 ml) was added dropwise 50% aqueous dimethylamine (2.63 g) with ice-cooling over a period of 10 minutes and the mixture was stirred for an additional 10 minutes. The mixture was heated at 50°-55° C. for 2 hours after an addition of 8-(2-chlorobenzyloxy)-2-methylimidazo[1,2-a]pyridine (7.6 g) thereto and then evaporated in vacuo. The residue was basified with aqueous sodium hydroxide and extracted with methylene chloride. The extract was washed with water, dried over magnesium sulfate and evaporated in vacuo. The residual solid was recrystallized from a mixture of diethyl ether and n-hexane to give 8-(2-chlorobenzyloxy)-3-dimethylaminomethyl-2-methylimidazo[1,2-a]pyridine (7.85 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04725601 |
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| Quelldatensatz | uspto-grants-1988_02 |
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| ORD ID | ord-92e60f8984b44a1db9d8ae0442b210af |
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| Quellennotiz | uspto-grants-1988_02 |
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