Processes for producing cycloalkylcarboxamido-pyridine benzoic acids

Abstract

The present invention relates to a process of providing the 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid in substantially free form (Compound 1).

Description

CROSS REFERENCE TO RELATED APPLICATIONS[0001]This application is a continuation-in-part of U.S. patent application Ser. No. 12 / 327,915, filed on Dec. 4, 2008, which claims the benefit of priority under 35 U.S.C. §119 to U.S. provisional patent application Ser. Nos. 61 / 012,181, filed Dec. 7, 2007, and 61 / 109,573, filed Oct. 30, 2008, the entire contents of all applications are incorporated herein by reference.TECHNICAL FIELD OF THE INVENTION[0002]The present invention relates to processes for the preparation of compounds useful for treating a CFTR mediated disease such as cystic fibrosis.BACKGROUND OF THE INVENTION[0003]CFTR is a cAMP / ATP-mediated anion channel that is expressed in a variety of cells types, including absorptive and secretory epithelia cells, where it regulates anion flux across the membrane, as well as the activity of other ion channels and proteins. In epithelia cells, normal functioning of CFTR is critical for the maintenance of electrolyte transport throughout the...

AI Technical Summary

Benefits of technology

[0011]As described herein, the present invention provides processes for preparing CFTR correctors useful in the treatment of cystic fibrosis. Such compounds include 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid (hereinafter “Compound 1”) which ha

Problems solved by technology

In contrast, individuals with two copies of the CF associated gene suffer from the debilitating and fatal effects of CF, including chronic lung disease.

In patients with cystic fibrosis, mutations in CFTR endogenously expressed in respiratory epithelia leads to reduced apical anion secretion causing an imbalance in ion and fluid transport.

The resulting decrease in anion transport contributes to enhanced mucus accumulation in the lung and the accompanying microbial infections that ultimately cause death in CF patients.

In addition to respiratory disease, CF patients typically suffer from gastrointestinal problems and pancreatic insufficiency that, if left untreated, results in death.

This results in the inability of the m

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