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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541475Generated: October 25, 2026

Potassium Carbonate → Methyl 2,4-dimethyl-5-(6-methyl-3,4,6,7-tetrahydropyrano[3,4-d]imidazol-2-yl)benzoate

https://huagongshe.com/reaction/541475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-bromo-6-methyldihydro-2H-pyran-3(4H)-oneHCID 68288204—
ReactantMethyl 5-carbamimidoyl-2,4-dimethylbenzoate hydrochlorideHCID 68288602—
Reactant5-bromo-2-methyldihydro-2H-pyran-4(3H)-oneHCID 68288732—
SolventAcetonitrileHCID 6342—
ProductMethyl 2,4-dimethyl-5-(6-methyl-3,4,6,7-tetrahydropyrano[3,4-d]imidazol-2-yl)benzoateHCID 682889709%

Reaction Conditions

Temperature75 °C

Reaction Steps

Into around-bottom flask, was placed a mixture of 4-bromo-6-methyldihydro-2H-pyran-3(4H)-one (compound 464.5) and 5-bromo-2-methyldihydro-2H-pyran-4(3H)-one (compound 464.6) (700 mg, 3.63 mmol) as a solution in acetonitrile (20 mL). Methyl 5-carbamimidoyl-2,4-dimethylbenzoate hydrochloride (compound 2.5, 750 mg) and potassium carbonate (1.00 g, 7.25 mmol) were added and the mixture was stirred overnight at 75° C. under nitrogen. The mixture was cooled and the solids were removed by filtration. The filtrate was concentrated in vacuo and the residue was purified by silica gel chromatography with ethyl acetate/petroleum ether (1:1) as the eluent to obtain the title compound as a yellow solid (100 mg, 9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-46fbf3561bb646d3b754f262613b652b
Source noteuspto-grants-2014_10