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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967500Generated: October 30, 2026

1,1'-Carbonyldiimidazole → 2-oxo-3-(1-benzylpiperidin-4-yl)-2,3-dihydro-1H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/967500

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridineHCID 22293245—
SolventTetrahydrofuranHCID 8028—
Product2-oxo-3-(1-benzylpiperidin-4-yl)-2,3-dihydro-1H-imidazo[4,5-c]pyridineHCID 2229317091.7%

Reaction Steps

A solution of 4-amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine (2.8 g, 9.9 mmol) and carbonyldiimidazole (3.0 g, 18.5 mmol) in tetrahydrofuran (100 mL) was refluxed overnight. The reaction was cooled, concentrated and partitioned between chloroform (500 mL) and saturated sodium carbonate (100 mL). The organic phase was dried over magnesium sulfate and concentrated to give the title compound (2.8 g). MS 209 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06953790B2
Source datasetuspto-grants-2005_10
ORD IDord-0c9e5c61f7744828ac04ff31ccc49dcb
Source noteuspto-grants-2005_10