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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453100Generated: October 31, 2026

Potassium Carbonate → 2,6-Difluoro-3-[3-(4-methoxyphenyl)-[1,2,4]thiadiazol-5-ylmethoxy]-benzamide

https://huagongshe.com/reaction/453100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2,6-Difluoro-3-hydroxybenzamideHCID 45120136—
Reactant5-Bromomethyl-3-(4-methoxyphenyl)-[1,2,4]thiadiazoleHCID 59549521—
SolventDimethylformamideHCID 6228—
Product2,6-Difluoro-3-[3-(4-methoxyphenyl)-[1,2,4]thiadiazol-5-ylmethoxy]-benzamideHCID 2523110730%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 5-bromomethyl-3-(4-methoxyphenyl)-[1,2,4]thiadiazole (0.048 g, 0.15 mmol) in DMF (2 ml) was added 2,6-difluoro-3-hydroxybenzamide (0.027 g, 0.15 mmol) and potassium carbonate (0.76 g, 0.55 mmol). The reaction mixture was stirred at 25° C. for 12 h under nitrogen atmosphere. After the completion of the reaction (TLC monitoring), the reaction mixture was evaporated to dryness under vacuum, added 30 ml water and extracted with ethyl acetate (3×20 ml). The combined organic layer was dried over Na2SO4, filtered and concentrated under vacuum. The crude residue was purified over silica gel (100-200 M, 50% EtOAc-Hexane) to get the desired product (0.011 g, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492414B2
Source datasetuspto-grants-2013_07
ORD IDord-3e4c7f56f18c4ccb8d3204e62967f375
Source noteuspto-grants-2013_07