Apotex Pharmachem Inc.

Laura Kaye Montemayor

Fan Wang

Daqing Che

Stephen E Horne

Bhaskar Reddy Guntoori

Yajun Zhao

Kiran Kumar Kothakonda

Uma Kotipalli

Sammy Chris Duncan

Alfredo Paul Ceccarelli

Minh T N Nguyen

Kaarina K Milnes

Kevin Wade Kells

There is provided processes for preparing Lubiprostone and intermediates thereof. Also provided are compounds, including intermediates for preparing Lubiprostone as well compositions comprising Lubiprostone and other compounds, including intermediates for preparing Lubiprostone and other compounds. (I) 

Methods of making lubiprostone and intermediates thereof

A novel process for the preparation of omeprazole and its enantiomers, such as esomeprazole, as well as the preparation of related 2-(2-pyridinylmethyl-sulphinyl)-1H-benzimidazoles, including pantoprazole, lansoprazole and rabeprazole, as recemates or single enantiomers, and their alkali or alkaline salts has been developed. The novel process involves the surprising discovery that protection of the free-base benzimidazole sulfoxide (e.g. omeprazole or esomeprazole), by reaction with an alkyl, aryl or aralkyl chloroformate following oxidation of the corresponding sulfide, eliminates the need for its direct isolation. Subsequent removal of the protecting group with a solution of alkali or alkaline earth alkoxide in a C1-C4 alcohol directly provides the corresponding salt. By eliminating the need to handle the free-base benzimidazole sulfoxide, this advantageous procedure provides increased chemical yields over processes described in the art.

Process for the preparation of esomeprazole and salts thereof

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St. George, Canada

Laura Kaye Montemayor