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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355072Generated: October 25, 2026

Ifenprodil hydrobromide → Ifenprodil

https://huagongshe.com/reaction/355072

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIfenprodil hydrobromideHCID 12613162—
ReactantAzane;hydrateHCID 12896473—
ProductIfenprodilHCID 3689—

Reaction Steps

In the practical preparation of the free ifenprodil, it is convenient to obtain the free ifenprodil directly from the reaction mixture, without once isolating ifenprodil hydrobromide, by adding ammonia water or a similar weakly basic substance to the filtrate from which solid matters including the catalyst have been removed, and concentrating the filtrate under reduced pressure to obtain the free compound as a residue which may, if desired, be purified by recrystallization from ethanol or isopropanol. The filtrate or mother liquor in the crystallization and/or recrystallization treatment may be subjected to silica gel column chromatography to recover a certain amount of ifenprodil. The total yields of ifenprodil can be increased by this after-treatment to about more than 90%. The free ifenprodil thus obtained may be reacted with an acid in a proper solvent to prepare an acid-addition salt with the acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377691
Source datasetuspto-grants-1983_03
ORD IDord-48259ad9489146e89d291ed00ffbe082
Source noteuspto-grants-1983_03