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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483491Generated: October 26, 2026

Sodium Hydroxide → 1-(1-Benzyl-4-piperidinyl)-3-methylcarbostyril hydrochloride

https://huagongshe.com/reaction/483491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantN-(alpha-methylcinnamoyl)-N-(1-benzyl-4-piperidinyl)anilineHCID 54264746—
SolventChlorobenzeneHCID 7964—
Product1-(1-Benzyl-4-piperidinyl)-3-methylcarbostyril hydrochlorideHCID 1903098074.2%

Reaction Conditions

Temperature110 °C

Reaction Steps

To grinded aluminum chloride (26 g) are added chlorobenzene (26 ml) and N-(α-methylcinnamoyl)-N-(1-benzyl-4-piperidinyl)aniline (8.7 g) and the mixture is heated at 110° C. for 1 hour. After cooling, the reaction mixture is poured into ice-water and made alkaline with an aqueous sodium hydroxide solution. After extraction with dichloromethane, the extract is concentrated and the resulting residue is purified by silica gel column chromatography (eluent; methylene chloride). The purified substance is converted into hydrochloride and then recrystallized from ethanol/water to give 1-(1-benzyl-4-piperidinyl)-3-methylcarbostyril hydrochloride (5.8 g) as colorless needles, m.p. 274°-276° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05225402
Source datasetuspto-grants-1993_07
ORD IDord-d10024505b724740bbaa71d89f1ce367
Source noteuspto-grants-1993_07