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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271872Generated: October 26, 2026

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

https://huagongshe.com/reaction/271872

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 numberUS07452903B2
Source datasetuspto-grants-2008_11
ORD IDord-93308ea79f34403e871e5a458a6d6141
Source noteuspto-grants-2008_11