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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768169Generated: November 2, 2026

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

https://huagongshe.com/reaction/1768169

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 numberUS07235545B2
Source datasetuspto-grants-2007_06
ORD IDord-d00901322f56426f8ad0bd9cd87f29af
Source noteuspto-grants-2007_06