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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1808663생성일: 2026년 10월 25일

Methanesulfonic Acid → Eprosartan Mesylate

https://huagongshe.com/reaction/1808663

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참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물EprosartanHCID 5281037—
용매IsopropanolHCID 3776—
생성물Eprosartan MesylateHCID 5282474—

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온도8 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08361507B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-aaf8478e97c44019b00c510f86452a37
출처 메모uspto-grants-2013_01