戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1808663作成日:2026年10月26日

Methanesulfonic Acid → Eprosartan Mesylate

https://huagongshe.com/reaction/1808663

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonic AcidHCID 6395—
反応物EprosartanHCID 5281037—
溶媒IsopropanolHCID 3776—
生成物Eprosartan MesylateHCID 5282474—

反応条件

温度8 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08361507B2
出典データセットuspto-grants-2013_01
ORD IDord-aaf8478e97c44019b00c510f86452a37
出典メモuspto-grants-2013_01