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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258855Generated: November 1, 2026

Sodium Carbonate → 4-chloro-3-{3-[4-(4-fluorobenzoyl)-1-piperidinyl]-propyl}-1,3-dihydro-2H-benzimidazol-2-one

https://huagongshe.com/reaction/258855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactantp-Fluorophenyl 4-piperidyl ketone hydrochlorideHCID 3084438—
Reactant3-(7-chloro-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl methanesulfonateHCID 21424814—
SolventDimethylformamideHCID 6228—
Product4-chloro-3-{3-[4-(4-fluorobenzoyl)-1-piperidinyl]-propyl}-1,3-dihydro-2H-benzimidazol-2-oneHCID 2142482818%

Reaction Conditions

Temperature55 °C

Reaction Steps

A mixture of 4.4 parts of 3-(7-chloro-2,3-dihydro-2-oxo-1H-benzimidazol-1-yl)propyl methanesulfonate, 3.4 parts of (4-fluorophenyl) (4-piperidinyl) methanone hydrochloride, 5 parts of sodium carbonate and 45 parts of N,N-dimethylformamide is stirred for 6 hours at 50-60° C. The reaction mixture is cooled and poured onto water. The product is extracted with 4-methyl-2-pentanone. The extract is dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 10% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from a mixture of 4-methyl-2-pentanone and 2,2'-oxybispropane, yielding 1 part (18%) of 4-chloro-3-{3-[4-(4-fluorobenzoyl)-1-piperidinyl]-propyl}-1,3-dihydro-2H-benzimidazol-2-one; mp. 138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04035369
Source datasetuspto-grants-1977_07
ORD IDord-1bb9798839e5417984d91c8b62c36276
Source noteuspto-grants-1977_07