Substituted 2-thio-3,5-dicyano-4-phenyl-6-aminopyridines and the use of the same

A method for the treatment of disorders of the urogenital region and cancer comprising administering to a patient in need thereof an effective amount of a compound of formula (I)

• in which
• n represents a number 2, 3 or 4,
• R1 represents hydrogen or (C1-C4)-alkyl
• and
• R2 represents pyridyl or thiazolyl which for its part may be substituted by (C1-C4)-alkyl, halogen, amino, dimethylamino, acetylamino, guanidino, pyridylamino, thienyl, furyl, imidazolyl, pyridyl, morpholinyl, thiomorpholinyl, piperdinyl, piperazinyl, N—(C1-C4)-alkylpiperazinyl, pyrrolidinyl, oxazolyl, isoxazolyl, pyrimidinyl, pyrazinyl, optionally (C1-C4)-alkyl-substituted thiazolyl or phenyl which is optionally substituted up to three times by halogen, (C1-C4)-alkyl or (C1-C4)-alkoxy,
• or a pharmaceutically acceptable salt, hydrate, hydrate of a salt, or solvate thereof.

A method for the treatment of inflammatory and neuroinflammatory disorders, neurodegenerative disorders and pain comprising administering to a patient in need thereof an effective amount of a compound of formula (I)

• in which
• n represents a number 2, 3 or 4,
• R1 represents hydrogen or (C1-C4)-alkyl
• and
• R2 represents pyridyl or thiazolyl which for its part may be substituted by (C1-C4)-alkyl, halogen, amino, dimethylamino, acetylamino, guanidino, pyridylamino, thienyl, furyl, imidazolyl, pyridyl, morpholinyl, thiomorpholinyl, piperidinyl, piperazinyl, N—(C1-C4)-alkylpiperazinyl, pyrrolidinyl, oxazolyl, isoxazolyl, pyrimidinyl, pyrazinyl, optionally (C1-C4)-alkyl-substituted thiazolyl or phenyl which is optionally substituted up to three times by halogen, (C1-C4)-alkyl or (C1-C4)-alkoxy,
• or a pharmaceutically acceptable salt, hydrate, hydrate of a salt, or solvate thereof.