HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22471Erstellt: 24. Oktober 2026
Diethyl Ether → 1-[3-(Dimethylamino)propyl]-3-phenyl-1H-pyrazolo[4,3-c]pyridine dihydrochloride
https://huagongshe.com/de/reaction/22471
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 3-Chloro-N,N-dimethyl-1-propanamine | HCID 66960 | — |
| Edukt | 3-Phenyl-1H-pyrazolo[4,3-c]pyridine | HCID 13801125 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 1-[3-(Dimethylamino)propyl]-3-phenyl-1H-pyrazolo[4,3-c]pyridine dihydrochloride | HCID 19930480 | — |
Reaktionsschritte
3-Phenyl-1H-pyrazolo[4,3-c]pyridine (3.90 g) was suspended in 50 ml of dimethylformamide and 60% NaH (1.0 g) was added. After stirring for 90 minutes, dimethylaminopropyl chloride (3.0 g) was added, and stirring was continued for 1 hour. At the end of this time the reaction was warmed to 55° and, after an additional 2 hours, an additional 0.50 g of dimethylaminopropyl chloride was added. Warming and stirring was continued for 1 hour, after which time the reaction mixture was distributed between ether and H2O. The organic phase was dried, evaporated, and purified by flash chromatography (5% triethylamine-ethyl acetate), giving an oil upon evaporation of the product-containing fractions. The hydrochloride was formed in ethereal HCl and recrystallized from methanol-ether to give 3.76 g of product, m.p. 237°-239°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05428169 |
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| Quelldatensatz | uspto-grants-1995_06 |
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| ORD ID | ord-4913146aa9ce408792d93d92a3809610 |
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| Quellennotiz | uspto-grants-1995_06 |
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