Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206442Generated: November 1, 2026

Hydrochloric Acid → Imidazo(1,5-a)pyridine

https://huagongshe.com/reaction/2206442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantMethanolHCID 887—
ReactantAcetonitrileHCID 6342—
Reactant2-PyridinecarboxaldehydeHCID 14273—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductImidazo(1,5-a)pyridineHCID 274090—

Reaction Steps

Imidazo[1,5-a]pyridine fluorophores were prepared by adding 1 equivalent (equiv) of 3 M hydrochloric acid in ethanol (an additional equivalent of acid was used in reactions with basic substrates) and picolinaldehyde or other 2-acylpyridine to 1 equiv of a 0.5 M solution of 1 equiv of primary amine in dry ethanol or acetonitrile and 1.5 equiv of formalin. The reaction was stirred at room temperature for the specified period of time (i.e., from about 15 min to about 12 hours) and monitored by analytical thin layer chromatography (TLC) (10% methanol in DCM) for the appearance of a blue fluorescent product spot by UV light. Crude reaction mixtures were concentrated in vacuo (˜15 Torr) and dried under high vacuum at 0.2 Torr (for from 2 to 12 hours).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371448B2
Source datasetuspto-grants-2016_06
ORD IDord-5cd34d59a06b42d38a2538ebb26b806c
Source noteuspto-grants-2016_06