Piperazine and piperidine compounds

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Having -c- – wherein x is chalcogen – bonded directly to...

Reexamination Certificate

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C514S254020, C514S318000, C514S321000, C514S333000, C514S338000, C544S364000, C544S368000, C546S194000, C546S198000, C546S256000, C546S270100, C546S271700

Reexamination Certificate

active

06911448

ABSTRACT:
The invention relates to a group of novel piperazine and piperidine derivatives of the formula wherein Y is hydrogen, halogen, alkyl (1-3C), or CN, CF3, OCF3, SCF3, alkoxy(1-3C), amino or mono- or dialkyl(1-3C) substituted amino or hydroxy, X is O, S, SO or SO2, ---Z represents —C, ═C or —N, R1and R2independently represent hydrogen or alkyl (1-3C), Q is benzyl or 2-, 3- or 4-pyridylmethyl, wich groups may be substited with one or more more substituents from the group halogen, nitro, cyano, amino, mono- or di (1-3C)alkylamino, (1-3C) alkoxy, CF3, OCF3, SCF3, (1-4C)-alkyl, (1-3C)alkylsulfonyl or hydroxy, and salts and prodrugs thereof. It has been found that these compounds have interesting pharmacological properties due to a combination of (partial) agonism towards the members of the dopamine D2-receptor subfamily and affinity for relevant serotonin and/or noradrenergic receptors

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patent: 01/85168 (2001-11-01), None
English Translation for Michiaki et al, JP 60-126275 (Jul. 1985).
Patent Abstract of Japan for JP 60-126275 (Jul. 1985).
Robichaud et al. in Annualr Reports in Medicinal Chemistry, vol. 35, p. 11-20 (2000).
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Perrone et al. J. Med. Chem. vol. 42, p. 490-496 (1999).
Perrone et al. Bioorganic & Medicinal Chemistry vol. 8, p.873-881 (2000).
International Search Report for PCT/EP 01/05320.

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