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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337520Generated: October 29, 2026

2-Chloropyridine-4-carbonyl chloride → 2-Chloro-N-[4-(3-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]pyridine-4-carboxamide

https://huagongshe.com/reaction/337520

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloropyridine-4-carbonyl chlorideHCID 2800003—
Reactant2-Amino-4-(3-furyl)thiazol-5-yl tetrahydropyran-4-yl ketoneHCID 86612473—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product2-Chloro-N-[4-(3-furyl)-5-(tetrahydropyran-4-ylcarbonyl)thiazol-2-yl]pyridine-4-carboxamideHCID 2314434436.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Compound 610 (100 mg, 0.359 mmol) was dissolved in pyridine (3 mL), and 6-chloroisonicotinoyl chloride (560 mg, 3.18 mmol) and DMAP (4.40 mg, 0.0360 mmol) were added thereto, followed by stirring at 80° C. for 3 hours. The reaction mixture was concentrated under reduced pressure, and the resulting residue was poured into a saturated aqueous solution of sodium hydrogencarbonate, and the precipitated solid was collected by filtration. The resulting solid was purified through silica gel column chromatography (hexane:ethyl acetate=3:1), followed by recrystallizing from a mixed solvent of ethanol and water to afford the entitled Compound 616 (54.5 mg, 36%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-f43e6ebf61fe4321a040068318638694
Source noteuspto-grants-2014_11