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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390708Generated: October 25, 2026

Cesium carbonate → (NZ)-N-(5-methyl-3-phenyl-1,3-thiazol-2-ylidene)pyrrolidine-1-carboxamide

https://huagongshe.com/reaction/390708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantIodobenzeneHCID 11575—
Reactant5-Chloro-1,10-phenanthrolineHCID 77865—
ReactantN-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamideHCID 47197229—
ReactantWater ammonium hydroxideHCID 86589665—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product(NZ)-N-(5-methyl-3-phenyl-1,3-thiazol-2-ylidene)pyrrolidine-1-carboxamideHCID 87449702—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a 4 mL vial equipped with a septum cap and stir bar was added N-(5-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carboxamide (21 mg, 0.1 mmol), copper(I) trifluoromethanesulfonate benzene complex (10 mg, 0.02 mmol), 5-chloro-1,10-phenanthroline (8.5 mg, 0.04 mmol) and cesium carbonate (38.9 mg, 0.12 mmol). The mixture was placed under a nitrogen atmosphere. Iodobenzene (0.12 mmol) in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the mixture. The reaction mixture was heated at 120° C. for overnight. A solution of concentrated ammonium hydroxide/water (1:2, 1 mL) was added and the mixture was filtered and solvent removed under reduced pressure. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383657B2
Source datasetuspto-grants-2013_02
ORD IDord-b9a1c7ad96754a8e8302465963d697d4
Source noteuspto-grants-2013_02