Abstract: The invention relates to tetrahydropyridinyldibenzazepine derivatives of the formula I ##STR1## wherein R.sub.1 is a substituent selected from the group consisting of hydrogen, halogen, and lower alkyl;R.sub.2 is selected from hydrogen, and unsubstituted or hydroxy substituted lower alkyl or lower alkenyl;X is O, S, or CH.sub.2 ;Y is HC.dbd.CH or S;or a pharmaceutically acceptable salt thereof.These compounds are dopamine antagonists and are therefore useful for the treatment of psychotic disorders such as schizophrenia, schizophreniform disorder, delusional disorder, acute manic states, senile and presenile psychotic states, toxic psychoses, psychoactive-substance induced psychoses, symptoms of severe restlessness, hyperexcitability and anxiety, motor disorders, among which Tourette's disorder and Huntington's chorea, nausea and vomiting, hiccup and dizziness.

Abstract: The invention relates to pyrazole derivative having formula I ##STR1## whereinR.sub.1 is ##STR2## and R.sub.2 is hydrogen, or R.sub.1 iswherein n is 1 or 2 and R.sub.2 is hydrogen or halogen; and R.sub.3 is bromine or iodine; or a pharmaceutically acceptable salt thereof.The compounds of this invention have muscarinic properties and can be used for the treatment of cognition disorders, for analgesia, and afore the treatment of cholinergic deficiencies.

Abstract: The invention relates to thiazole derivatives with the general formula I ##STR1## wherein R.sup.1 is halogen, CF.sub.3, CN, NO.sub.2, OH or C.sub.1 -C.sub.6 alkoxy;R.sup.2 is hydrogen, C.sub.1 -C.sub.6 alkyl, C.sub.1 -C.sub.6 alkoxy, aryl, C.sub.6 -C.sub.13 aralkyl, an unsubstituted amino group, a substituted amino group, or an amino group which is part of a 5- or 6-membered ring;R.sup.3 is C.sub.1 -C.sub.6 hydrocarbon, C.sub.6 -C.sub.13 aralkyl, C.sub.2 -C.sub.7 alkoxyalkyl or C.sub.1 -C.sub.13 acyl; and their pharmaceutically acceptable acid addition salts.These new compounds have .alpha..sub.2 -antagonist activity without dopamine agonist activity and as such are specifically useful for the treatment of depression and other related illnesses, e.g. for treating patients with anxiety disorders and cognitive disturbances.

Abstract: The invention relates to aminoethylthiazole and aminoethyloxazole derivatives with the general formula I ##STR1## wherein X is O or S;ALK is a hydrocarbyl (C.sub.2 -C.sub.6) group;R.sup.1 is a substituted or unsubstituted aryl group;R.sup.2 is a hydrogen, a hydrocarbyl (C.sub.1 -C.sub.6) group or an aralkyl (C.sub.7 -C.sub.13) group;R.sup.3 is a substituted or unsubstituted amino group;or their pharmaceutically acceptable acid addition salts.These new compounds are dopamine agonists with selectively for pre-synaptic dopamine receptors and, as such, are useful as anti-psychotics in the treatment of schizophrenia. The compounds are also useful in the treatment of hypertension, Parkinsonism and for the conditions of hyperprolactineamia, e.g. galactorrhea, menstrual disorders and amenorrhea.

Abstract: The invention relates to tetrahydronaphthalene and indane derivatives with the general formula I: ##STR1## wherein R.sup.1 represents zero to four substituents, which may be the same or different and are selected from OH, halogen, NO.sub.2, CN, CF.sub.3, C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkoxy and unsubstituted or C.sub.1 -C.sub.4 alkyl substituted amino;R.sup.2 represents C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkenyl and C.sub.1 -C.sub.4 alkynyl which may be substituted by halogen;R.sup.3 and R.sup.4 represent independently H, C.sub.1 -C.sub.4 alkyl or form together with the nitrogen atom a 5- or 6-membered ring;n has the value 0 or 1;ALK is an aliphatic hydrocarbon with 1-8 carbon atoms and their pharmaceutically acceptable salts.These new compounds are typical monoamine reuptake blockers with additional .alpha..sub.2 antagonist activity and show strong anti-depressant activity without being sedative.

Abstract: The present invention relates to new amino-thiazole and amino-oxazole derivatives of the general formula: ##STR1## wherein: R represents hydrogen, a lower alkyl group with 1 to 4 carbon atoms, a lower alkenyl group, a phenyl-alkyl (1-4 C), furanyl-alkyl (1-4 C) or thienyl-alkyl (1.varies.4 C) group;X represents sulphur or oxygen;R.sub.1 and R.sub.2 represent hydrogen or alkyl (1-4 C), andthe dotted line represents an optional extra bond,as well as pharmaceutically acceptable acid addition salts thereof, having potent dopamine-agonist activity.

Abstract: The present invention deals with dibenzo-oxocin-, dibenzo-thiocin-, dibenzo-azocin- and dibenzocyclo-octenamine derivatives suitable for use as antipsychotic compounds without extra-pyrimidal side-effects.

Abstract: The present invention relates to novel benzo(b) bicyclo[3.3.1]nones of the general formula I: ##STR1## and a salt or nitrogen oxide thereof, in which R.sub.1 and R.sub.2 stand for hydrogen, alkyl of 1-6 carbon atoms, alkenyl of 1-6 carbon atoms, an optionally substituted aralkyl group or an acyl group orR.sub.1 and R.sub.2 together with the nitrogen atom represent a heterocyclic 5- or 6-membered ringR.sub.3 is a free, etherified or esterified hydroxy,X and Y stand for hydrogen, hydroxy, halogen, alkyl or alkoxy of 1-6 C-atoms, nitro, CF.sub.3 or an acyloxy group, having valuable biological activities, particularly anorectic activity.

Abstract: The present invention relates to new amino-thiazole and amino-oxazole derivatives of the general formula: ##STR1## wherein: R represents hydrogen, a lower alkyl group with 1 to 4 carbon atoms, a lower alkenyl group, a phenyl-alkyl (1-4 C), furanyl-alkyl (1-4 C) or thienyl-alkyl (1-4 C) group;X represents sulphur or oxygen;R.sub.1 and R.sub.2 represent hydrogen or alkyl (1-4 C), and the dotted line represents an optional extra bond,as well as pharmaceutically acceptable acid addition salts thereof, having potent dopamine-agonist activity.