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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254442Generated: October 27, 2026

4-Toluenesulfonyl chloride → Azilsartan Medoxomil

https://huagongshe.com/reaction/254442

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Hydroxymethyl)-5-methyl-1,3-dioxol-2-oneHCID 10510878—
ReactantAzilsartanHCID 135415867—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductAzilsartan MedoxomilHCID 13540964295%

Reaction Conditions

Temperature10 °C

Reaction Steps

To a solution of 2-ethoxy-1-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}-1H-benzimidazole-7-carboxylic acid (9.0 g) and 4-hydroxymethyl-5-methyl-1,3-dioxol-2-one (3.08 g) in N,N-dimethylacetamide (100 mL) were added p-toluenesulfonyl chloride (4.13 g), N,N-dimethylaminopyridine (0.48 g) and potassium carbonate (3.54 g) under ice-cooling and the mixture was stirred at about 10° C. for 3 hrs. After adjusting the pH of the mixture to about 5, the mixture was crystallized by adding water (72 mL) to give crystals as a solvate. The isolated crystals were suspended in a mixture of water (63 mL) and acetone (27 mL) and the suspension was stirred at about 35° C. for 2 hrs. After stirring under ice-cooling for 2 hrs, the crystals were collected by filtration and the crystals were washed with water (18 mL) and dried under reduced pressure at 40° C. to give the title compound (10.6 g, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875637B2
Source datasetuspto-grants-2011_01
ORD IDord-dd936233f3dd415481663452159e4b27
Source noteuspto-grants-2011_01