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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554019Generated: October 31, 2026

Potassium Iodide → Tritylolmesartan medoxomil

https://huagongshe.com/reaction/554019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Chloromethyl)-5-methyl-1,3-dioxol-2-oneHCID 9855518—
Reactant4-(2-Hydroxypropan-2-yl)-2-propyl-1-({2'-[1-(triphenylmethyl)-1H-tetrazol-5-yl][1,1'-biphenyl]-4-yl}methyl)-1H-imidazole-5-carboxylic acidHCID 19036305—
SolventAcetoneHCID 180—
SolventTolueneHCID 1140—
ProductTritylolmesartan medoxomilHCID 19036162—

Reaction Steps

4-(1-Hydroxy-1-methylethyl)-2-propyl-1-{4-[2-(trityltetrazol-5-yl)phenyl]phenyl}methylimidazole-5-carboxylic acid dehydrate (100 g) was suspended in acetone (1 L) & heated to reflux; the solution obtained was added to suspension of potassium carbonate (15 g), potassium iodide (6 g) & 4-chloromethyl-5-methyl-1,3-dioxol-2-one (35 g) in acetone (500 mL) at reflux temperature. Reaction mass was refluxed for 2-6 hrs. After competition of reaction, the reaction mass was filtered & the acetone was distilled from combined mother liquor. The residue obtained was dissolved in toluene (1 L) toluene layer was washed with brine (3×250 mL). Toluene was removed under reduced pressure & residue thus obtained was recrystallized from methanol to give trityl Olmesartan

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048904B2
Source datasetuspto-grants-2011_11
ORD IDord-27a33cadc84643d582af36ff21d06704
Source noteuspto-grants-2011_11