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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450522Generated: October 30, 2026

Potassium Carbonate → HCID 42603358, compound

https://huagongshe.com/reaction/450522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
ReactantHCID 42603083HCID 42603083—
CatalystDimethylformamideHCID 6228—
SolventAcetonitrileHCID 6342—
ProductHCID 42603358HCID 42603358—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 1-[(3,4-dichlorophenyl)methyl]-N-(3-hydroxyphenyl)-5-methyl-1H-1,2,3-triazole-4-carboxamide (Example 31) (0.1 g, 0.29 mmol) in acetonitrile (10 mL) and a couple of drops of DMF, were added 2-[(2-bromoethyl)oxy]tetrahydro-2H-pyran (0.09 μl, 2 eq) and potassium carbonate (0.08 g, 2 eq). The reaction was heated at 40° C. for 1 week. After evaporation, the residue was dissolved in DCM, washed with water and dried over sodium sulphate. After purification by flash chromatography eluting with DCM/MeOH, 98/2, the crude compound was dissolved in MeOH and some drops of a concentrated HCl solution in AcOEt were added and the solution was stirred at room temperature for 3 hours. After evaporation, the compound was recrystallised (twice) from methanol and washed with a mixture of ether and pentane. The title compound was obtained as a green solid (45 mg, 36%). HRMS calculated for C19H18Cl2N4O3 (M+H)+421.0834, found: 421.0804, Rt: 2.87 min. MP: 144.9° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486977B2
Source datasetuspto-grants-2013_07
ORD IDord-5e20668cea6c4b2a97a1e29dc8d410cd
Source noteuspto-grants-2013_07