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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365942Generated: 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/1365942

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 numberUS07893052B2
Source datasetuspto-grants-2011_02
ORD IDord-d69b0a0f8daa4b58932c380da90cc94e
Source noteuspto-grants-2011_02