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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492253Generated: October 30, 2026

Pyridine → HCID 69057960, compound

https://huagongshe.com/reaction/492253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant5-Hydroxyindole-2-carboxylic acidHCID 88958—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Aminopyridine-2-carbonitrileHCID 3871395—
Reactant1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chlorideHCID 10986715—
SolventChloroformHCID 6212—
ProductHCID 69057960HCID 69057960—

Reaction Steps

At 0° C., 2-chloro-1,3-dimethyl-imidazolinium chloride (1.0 g) was added to a chloroform (6.0 mL)/pyridine (6.0 mL) mixed solution of 5-amino-2-cyanopyridine (500 mg) and 5-hydroxyindole-2-carboxylic acid (1.1 g), and stirred for 3 hours, and further stirred overnight at room temperature. Aqueous sodium hydrogencarbonate solution was added to the reaction liquid to stop the reaction, and this was extracted with chloroform. The organic layer was washed with water and saturated saline water, and then dried with anhydrous sodium sulfate. The organic layer was concentrated under reduced pressure, and the resulting crystal was washed with chloroform to obtain the entitled compound (1.4 g) as a pale red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531668B2
Source datasetuspto-grants-2009_05
ORD IDord-dd1afc25339d4bd0a78c093b7d8b3fc2
Source noteuspto-grants-2009_05