FIELD: chemistry.
SUBSTANCE: present invention refers to the new compounds of formula I: whereat : a is 0 or 1; R1 means halogen; b is 0 or 1; R2 means halogen; m is 0 or 1; R4 is selected from hydrogen, (1-4C)alkyl and (3-4C)cycloalkyl; s is 0, 1 or 2; Ar1 is phenylen group or (3-5C)heteroarylen group containing 1 or 2 heteroatom independently selected from oxygen, nitrogen or sulphur; whereat phenylen or heteroarylen group is substituted with (R5)q whereat q is 0 or integer number from 1 to 4 and every R5 is independently selected from halogen or (1-4C)alkoxy; t is 0, 1 or 2; n is 0 or integer number from 1 to 3; p is 0 or 1; and R7 and R8 independently represent hydrogen or (1-4C)alkyl ; or to their pharmaceutically acceptable salts or solvates, or to their stereoisomers. The invention refers also to the pharmaceutical composition, method for preparation of compounds as in any of claims 1-13, to the medicinal preparation as well as to the application of the compounds.
EFFECT: obtaining of new bioactive compounds active as muscarinic receptor antagonists.
27 cl, 34 ex
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Authors
Dates
2009-09-10—Published
2005-03-10—Filed