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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913143Generated: November 2, 2026

4-Piperidinecarboxylic acid → 2-(piperidin-4-yl)-1H-1,3-benzodiazole

https://huagongshe.com/reaction/1913143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantO-PhenylenediamineHCID 7243—
ReactantSodium HydroxideHCID 14798—
SolventHydrochloric AcidHCID 313—
Product2-(piperidin-4-yl)-1H-1,3-benzodiazoleHCID 71581038%

Reaction Steps

This compound is synthesized as described by adaptation of the following reference: J. Heterocyclic Chem., 1989, 26, 54. A mixture of benzene-1,2-diamine (12.6 g, 116 mmol), piperidine-4-carboxylic acid (15 g, 116 mmol) and 4M aqueous HCl (250 mL) is stirred and heated under reflux for 48 h. The reaction mixture is cooled to room temperature and is made basic by addition of 5M aqueous NaOH. The precipitate formed is collected by suction filtration, washed with water and dried in the vacuum oven to afford 8.8 g (38%) of 2-(piperidin-4-yl)-1H-benzimidazole. m/z=202 [M++H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609696B2
Source datasetuspto-grants-2013_12
ORD IDord-928d8aeccbed413496fc2d1e4e3f0f88
Source noteuspto-grants-2013_12