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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktSodium hydrideHCID 24758—
Edukt3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
Edukt3-Phenyl-1H-pyrazolo[4,3-c]pyridineHCID 13801125—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt1-[3-(Dimethylamino)propyl]-3-phenyl-1H-pyrazolo[4,3-c]pyridine dihydrochlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428169
Quelldatensatzuspto-grants-1995_06
ORD IDord-4913146aa9ce408792d93d92a3809610
Quellennotizuspto-grants-1995_06