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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716603Generated: November 3, 2026

Hydrochloric Acid → 2,6-dimethyl-3-piperidin-4-yl-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/1716603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-[4-(2,6-Dimethyl-imidazo[4,5-c]-pyridin-3-yl)-piperidin-1-yl]-ethanoneHCID 68514583—
SolventEthanolHCID 702—
Product2,6-dimethyl-3-piperidin-4-yl-3H-imidazo[4,5-c]pyridineHCID 5885229277%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 1-[4-(2,6-dimethyl-imidazo[4,5-c]-pyridin-3-yl)-piperidin-1-yl]-ethanone) 20 mg, 0.0735 mmol) in ethanol (0.5 mL) was treated with concentrated HCl (0.5 mL). The reaction mixture was heated at 100° C. for 18 h. The solvent was evaporated and the mixture was diluted with water (2 mL). The mixture was washed with diethyl ether and the aqueous phase was adjusted to pH=10 by addition of a solution of 25% aqueous NaOH. The aqueous mixture was extracted with CH2Cl2 (5×10 mL). The combined extracts were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to afford 2,6-dimethyl-3-piperidin-4-yl-3H-imidazo[4,5-c]pyridine (13 mg, 77%) as a light yellow solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803816B2
Source datasetuspto-grants-2010_09
ORD IDord-9156f7693b684510afab1fd0d5f13729
Source noteuspto-grants-2010_09