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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35608Generated: October 24, 2026

Ammonia → 5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole

https://huagongshe.com/en/reaction/35608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantButyric AcidHCID 264—
ReactantHydrochloric AcidHCID 313—
ReactantEthyl 3,4-DiaminobenzoateHCID 458855—
Reactant4-[3-(1-Piperidinylmethyl)phenoxy]butanoic acidHCID 14221805—
SolventWaterHCID 962—
Product5-Ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazoleHCID 21294573—

Reaction Steps

A mixture of ethyl 3,4-diaminobenzoate (0.9 g), 4-(3-piperidinomethylphenoxy)butyric acid (2.1 g) prepared as described in Example 42 and 4N hydrochloric acid (6 ml) was heated and stirred under reflux for 90 minutes. A further portion of the butyric acid (2.1 g) and of 4N hydrochloric acid (6 ml) was added and the mixture heated under reflux for 90 minutes. The reaction mixture was cooled and poured into water (10 volumes). Aqueous ammonia (S.G. 0.880) was added until the solution was alkaline and the mixture was extracted with ethyl acetate. The extracts were washed with water, dried and on removal of the solvent gave a residue which was purified by preparative layer chromatography on silica gel plates using a 1:1 mixture of dichloromethane and methanol to give 5-ethoxycarbonyl-2-[3-(3-piperidinomethylphenoxy)propyl]benzimidazole as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04767769
Source datasetuspto-grants-1988_08
ORD IDord-6ca45163fe16494d994857b3c6d78a42
Source noteuspto-grants-1988_08