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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911415Generated: November 3, 2026

Cesium carbonate → Ethyl 5-(3,3-dimethylpiperazin-1-yl)thiophene-2-carboxylate

https://huagongshe.com/reaction/1911415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantEthyl 5-bromothiophene-2-carboxylateHCID 605723—
ReactantBinap, (A+-)-HCID 634876—
Reactant2,2-DimethylpiperazineHCID 14664186—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
ProductEthyl 5-(3,3-dimethylpiperazin-1-yl)thiophene-2-carboxylateHCID 6658967936.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

Palladium(II) acetate (0.112 g, 0.50 mmol) was added to ethyl 5-bromothiophene-2-carboxylate (1.175 g, 5 mmol), 2,2-dimethyl-piperazine (0.571 g, 5.00 mmol), rac-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.311 g, 0.50 mmol) and cesium carbonate (2.281 g, 7.00 mmol) in toluene (50.0 ml) at 20° C. under nitrogen. The resulting suspension was stirred at 110° C. for 23 h. The crude product was purified by ion exchange chromatography, using a SCX2 column. The crude material was dissolved in methanol and then applied to the column. The desired product was eluted from the column using 2M NH3 in methanol and pure fractions were evaporated to dryness to afford the crude product as a brown solid. This material was further purified by silica column chromatography, eluting with a gradient of 0 to 4% MeOH in DCM. Pure fractions were evaporated to dryness to afford ethyl 5-(3,3-dimethylpiperazin-1-yl)thiophene-2-carboxylate (0.484 g, 36.1%) as a brown gum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-73b9767268854222ab628cce72d8e7d3
Source noteuspto-grants-2013_12