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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 928826Generated: October 31, 2026

Hantzsch ester → HCID 178517028, compound

https://huagongshe.com/reaction/928826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHantzsch esterHCID 70849—
Reactant6-(Trifluoromethyl)pyridine-3-carboxaldehydeHCID 2777762—
Reactant6-Bromo-4-hydroxyquinolin-2(1H)-oneHCID 54689446—
Reactant4-((6-Bromo-2,4-dichloroquinolin-3-yl)methyl)benzonitrileHCID 86715622—
SolventPyridineHCID 1049—
SolventIsopropanolHCID 3776—
ProductHCID 178517028HCID 178517028—

Reaction Steps

6-Bromo-4-hydroxyquinolin-2(1H)-one (3.2 g, 18.3 mmol, Intermediate 44: step a), 6-(trifluoromethyl)nicotinaldehyde (4.0 g, 16.7 mmol), and diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate (4.2 g, 16.7 mmol), in pyridine (34 mL) were heated to 105° C. for 3 hours. The solution was allowed to cool to ambient temperature, resulting in the formation of solid. Minimal isopropanol was added to the mixture and the slurry was stirred for 1 hour, sonicated, and filtered. The filtered solids were rinsed with isopropanol and dried under continuous air flow to provide the title compound as an off-white solid. Additional product was recrystallized from the filtrate, filtered, and rinsed with isopropanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290476B2
Source datasetuspto-grants-2016_03
ORD IDord-11015ede2ee94c10a4909aeb12956f56
Source noteuspto-grants-2016_03