Bridged piperidine derivatives
Abstract
The present invention relates to a compound of formula wherein HetAr is a five or six membered hetaryl group, containing one, two or three heteroatoms, selected from N, O or S; R 1 is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, or lower alkoxy; R 2 is lower alkyl substituted by halogen, —CH 2 —C 3-6 -cycloalkyl, substituted by one or two substituents, selected from lower alkyl substituted by halogen or halogen, or is lower alkenyl substituted by halogen; R 3 is hydrogen, lower alkyl substituted by halogen, lower alkyl, halogen, C 3-6 -cycloalkyl or lower alkyl substituted by hydroxy; n is 1 or 2; for n=2, R 1 can be independent to each other; Y is CH or N; or to a pharmaceutically active acid addition salt thereof, to a racemic mixture or its corresponding enantiomer and/or optical isomer and/or stereoisomer thereof. The compounds may be used for the treatment of Alzheimer's disease, cerebral amyloid angiopathy, hereditary cerebral hemorrhage with amyloidosis, Dutch-type (HCHWA-D), multi-infarct dementia, dementia pugilistica or Down syndrome.
Claims
exact text as granted — not AI-modified1 . A compound of formula
wherein
HetAr is a five or six membered hetaryl group, containing one, two or three heteroatoms, selected from N, O or S;
R 1 is hydrogen, lower alkyl, lower alkyl substituted by halogen, halogen, or lower alkoxy;
R 2 is lower alkyl substituted by halogen, —CH 2 —C 3-6 -cycloalkyl, substituted by one or two substituents, selected from lower alkyl substituted by halogen or halogen, or is lower alkenyl substituted by halogen;
R 3 is hydrogen, lower alkyl substituted by halogen, lower alkyl, halogen, C 3-6 -cycloalkyl or lower alkyl substituted by hydroxy;
n is 1 or 2; for n=2, R 1 can be independent to each other;
Y is CH or N;
or a pharmaceutically active acid addition salt thereof, racemic mixture or its corresponding enantiomer and/or optical isomer and/or stereoisomer thereof.
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