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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808663Generated: October 25, 2026

Methanesulfonic Acid → Eprosartan Mesylate

https://huagongshe.com/reaction/1808663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantEprosartanHCID 5281037—
SolventIsopropanolHCID 3776—
ProductEprosartan MesylateHCID 5282474—

Reaction Conditions

Temperature8 °C

Reaction Steps

As per the process described and exemplified in the U.S. Pat. No. 5,185,351 (herein after referred to as the '351 patent), eprosartan free base (obtained as per the processes described in example I of the '351 patent) is suspended in isopropyl alcohol under stirring at about 8° C., methanesulfonic acid is added rapidly to the stirred suspension, the mass cooled to 3° C. and the precipitated solid collected to give crude eprosartan mesylate. The crude eprosartan mesylate is further purified by dissolving crude eprosartan mesylate in acetic acid at 80° C., filtered through a hyflow bed at 80° C., the solution cooled slowly to 25° C. followed by stirring and then the precipitated solid is collected by adding ethyl acetate as an anti-solvent to give eprosartan mesylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08361507B2
Source datasetuspto-grants-2013_01
ORD IDord-aaf8478e97c44019b00c510f86452a37
Source noteuspto-grants-2013_01