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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39765Generated: October 26, 2026

Dimethylformamide → HCID 59398235, compound

https://huagongshe.com/reaction/39765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethylthio)-thiopheneHCID 12201119—
ReactantHCID 59397947HCID 59397947—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 59398235HCID 5939823568.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

To 4 mL of an N,N-dimethylformamide solution containing 0.29 g of ethyl 4-(3-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)propyl)piperidine-4-carboxylate, 0.25 g of potassium carbonate and 0.20 g of 2-(2-bromoethylthio)thiophene were added and stirred at 60-70° C. for 2 hours. Water and ethyl acetate were added, the organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layer and extracts were combined, washed with aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent; chloroform:methanol=100:1] to give 0.27 g of ethyl 4-(3-(7-methoxy-4-methyl-2-oxoquinolin-1(2H)-yl)propyl)-1-(2-(2-thienylthio)ethyl)piperidine-4-carboxylate as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524738B2
Source datasetuspto-grants-2013_09
ORD IDord-b9a8e452c6fa461f88144e709f3e4a15
Source noteuspto-grants-2013_09