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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364088Generated: November 1, 2026

Cesium carbonate → HCID 66743327, compound

https://huagongshe.com/reaction/2364088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantDimethylacetamideHCID 31374—
Reactant4-(Bromomethyl)pyridine hbrHCID 12752219—
ReactantMethyl 5-bromo-3-(2,2,2-trifluoroacetamido)thiophene-2-carboxylateHCID 56965789—
SolventWaterHCID 962—
ProductHCID 66743327HCID 6674332748.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl 5-bromo-3-[(trifluoroacetyl)amino]thiophene-2-carboxylate (500 mg, 1.51 mmol), 4-(bromomethyl)pyridine hydrobromide (457 mg, 1.81 mmol), cesium carbonate (1.72 g, 5.29 mmol) and DMA (15 mL) was stirred at 80° C. for 2 h. Then, water was added to quench the reaction. The organic materials were extracted with EtOAc. The combined extracts were washed with water and brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was dissolved in MeOH (5 mL). To the solution were added potassium carbonate (500 mg) and water (2.5 mL). The mixture was stirred at room temperature for 2 h. After removal of the solvent at reduced pressure, the organic materials were extracted with EtOAc. The combined extracts were washed with brine, dried over Na2SO4 and filtered. After removal of the solvent at reduced pressure, the residue was purified by column chromatography (Purif, silica gel, hexane to 50:50 hexane/EtOAc) to give the title compound (238 mg, 48%) as a yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-ac3fd41a49a2406f8791a897f807f97e
Source noteuspto-grants-2014_04