Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051901Generated: November 1, 2026

Potassium Carbonate → 1-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-one

https://huagongshe.com/reaction/1051901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Chlorophenylboronic acidHCID 74299—
Reactant4-(4-(4-Chlorophenyl)-2-((2-oxopyrrolidin-1-yl)methyl)thiazol-5-yl)benzenesulfonamideHCID 71735399—
ReactantHCID 89813516HCID 89813516—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
Product1-((4-(4-Chlorophenyl)thiazol-2-yl)methyl)pyrrolidin-2-oneHCID 8981333586.6%

Reaction Conditions

Temperature97.5 °C

Reaction Steps

(4-chlorophenyl) boronic acid (0.22 g, 1.42 mmol) and potassium carbonate (0.41 g, 2.97 mmol) were added to a solution of 1-((4-bromothiazol-2-yl)methyl)pyrrolidin-2-one (Step-1 of Compound 103, 0.31 g, 1.18 mmol) in a mixture of toluene:ethanol (5:15 ml) in a tube at 25° C. Nitrogen gas was bubbled through the reaction mixture for 15 minutes. Tetrakis(triphenylphosphine)(0)palladium (0.07 g, 0.06 mmol) was then added to the reaction mixture under nitrogen atmosphere and the tube was sealed. The reaction mixture was heated at 95-100° C. for lhr under stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and filtered through celite. The celite cake was washed with ethanol (20 ml). The combined filtrate was concentrated under reduced pressure to obtain a crude product, which was then purified by column chromatography using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.3 g, 86.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-a97c1b8094254b22a7901fc5afea14ec
Source noteuspto-grants-2016_07