Claims
- 1. An N-substituted 3-azabicycloalkane of the formula I ##STR7## wherein B is a 3-, 5- or 6-membered ring which, in addition to carbon atoms, may contain 1 nitrogen atom and/or 1 oxygen atom and optionally a double bond,
- R.sup.1 is phenyl which is unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl, hydroxyl, C.sub.1 -C.sub.4 -alkoxy, amino, monomethylamino, dimethylamino, cyano or nitro groups,
- R.sup.2 is hydrogen, C.sub.1 -C.sub.4 -alkyl, or phenyl which is unsubstituted or substituted by halogen, methoxy, hydroxyl or amino,
- n is 0, 1, 2, 3, or 4,
- R.sup.3 is hydrogen, hydroxyl, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy or,
- is together with the adjacent carbon atom, a C.dbd.O or C.dbd.S group,
- one of X and Y is a carbon atom, CH or CH.sub.2, and the other is a NH or C.sub.1 -C.sub.4 -alkyl-N group or a nitrogen atom,
- Z is a C.dbd.O group, C.dbd.S group or
- is a CH or CH.sub.2 group in which one hydrogen atom can be replaced by a hydroxyl, amino or C.sub.1 -C.sub.4 -alkoxy group or a halogen atom, and
- A is C.sub.1 -C.sub.4 -alkylamino, or
- is a C.sub.3 -C.sub.4 -alkylene group which is linked to Y and which may contain one or two non-cumulative double bonds and where the ring may be monosubstituted either by a fluorine or chlorine atom or a methyl, methoxy, nitro or amino group or, in the case of a benzene ring, the latter may be mono-, di- or trisubstituted by fluorine or chlorine atoms or methyl, trifluoromethyl, nitro, hydroxyl, methoxy, amino, monomethyl- or dimethylamino groups,
- and where the ring on the right of the formula I may have on nitrogen atom No. 1 a hydrogen atom or a C.sub.1 -C.sub.4 -alkyl group and may contain 1, 2 or 3 non-cumulative double bonds,
- or salts thereof with physiologically tolerated acids.
- 2. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein R.sup.1 is phenyl which is unsubstituted or mono- or disubstituted by fluorine, chlorine, methoxy, nitro, trifluoromethyl, hydroxyl or amino, or salts thereof with physiologically tolerated acids.
- 3. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein R.sup.2 is hydrogen or methyl, or salts thereof with physiologically tolerated acids.
- 4. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein R.sup.3 is methyl or hydroxyl, or salts thereof with physiologically tolerated acids.
- 5. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein n is 2, or salts thereof with physiologically tolerated acids.
- 6. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 3, wherein
- B is a 3-, 5- or 6-membered ring which may contain a double bond,
- R.sup.1 is phenyl which is unsubstituted or mono- or disubstituted by halogen atoms, C.sub.1 -C.sub.4 -alkyl, trifluoromethyl, cyano or nitro groups,
- R.sup.2 is hydrogen,
- n is 2, 3, or 4,
- Z is a C.dbd.O group, or a CH or CH.sub.2 group, and
- A is C.sub.1 -C.sub.4 -alkylamino, or
- is a C.sub.3 -C.sub.4 -akylene group which is linked to Y and which may contain one or two non-cumulative double bonds and in the case of a benzene ring, the latter may be mono-, di- or trisubstituted by fluorine or chlorine atoms or methyl, trifluoromethyl, nitro, hydroxyl or methoxy groups,
- or salts thereof with physiologically tolerated acids.
- 7. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein
- one of X and Y is a carbon atom, CH or CH.sub.2, and the other is a NH or C.sub.1 -C.sub.4 -alkyl-N group or a nitrogen atom,
- Z is a C.dbd.O group, C.dbd.S group or
- is a CH or CH.sub.2 group in which one hydrogen atom can be replaced by a hydroxyl, amino or C.sub.1 -C.sub.4 -alkoxy group or a halogen atom, and
- A is C.sub.1 -C.sub.4 -alkylamino, or
- is a C.sub.3 -C.sub.4 -akylene group which is linked to Y and which may contain one or two non-cumulative double bonds and where the ring may be monosubstituted either by a fluorine or chlorine atom or a methyl, methoxy, nitro or amino group or, in the case of a benzene ring, the latter may be mono-, di- or trisubstituted by fluorine or chlorine atoms or methyl, trifluoromethyl, nitro, hydroxyl, methoxy, amino, monomethyl- or dimethylamino groups,
- or salts thereof with physiologically tolerated acids.
- 8. An N-substituted 3-azabicycloalkane of the formula I as defined in claim 1, wherein
- one of X and Y is a carbon atom, CH or CH.sub.2, and the other is a NH or C.sub.1 -C.sub.4 -alkyl-N group or a nitrogen atom,
- Z is a C.dbd.O group, C.dbd.S group or
- is a CH or CH.sub.2 group in which one hydrogen atom can be replaced by a hydroxyl, amino or C.sub.1 -C.sub.4 -alkoxy group or a halogen atom, and
- A is C.sub.1 -C.sub.4 -alkylamino, or
- is a C.sub.3 -C.sub.4 -akylene group which is linked to Y and which may contain one or two non-cumulative double bonds and where the ring may be monosubstituted either by a fluorine or chlorine atom or a methyl, methoxy, nitro or amino group or, in the case of a benzene ring, the latter may be mono-, di- or trisubstituted by fluorine or chlorine atoms or methyl, trifluoromethyl, nitro, hydroxyl, methoxy, amino, monomethyl- or dimethylamino groups,
- or salts thereof with physiologically tolerated acids.
- 9. A therapeutic composition comprising an N-substituted 3-azabicycloalkane of the formula I as defined in claim 1 or its pharmacologically suitable acid addition salt and conventional excipients and diluents.
Priority Claims (1)
Number |
Date |
Country |
Kind |
43 38 396 |
Nov 1993 |
DEX |
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Parent Case Info
This is a 371 application of PCT/EP94/03583, filed Oct. 31, 1994.
PCT Information
Filing Document |
Filing Date |
Country |
Kind |
102e Date |
371c Date |
PCT/EP94/03583 |
10/31/1994 |
|
|
5/6/1996 |
5/6/1996 |
Publishing Document |
Publishing Date |
Country |
Kind |
WO95/13279 |
5/18/1995 |
|
|
US Referenced Citations (2)
Number |
Name |
Date |
Kind |
3960861 |
Danilewicz et al. |
Jun 1976 |
|
5049564 |
DeBernardis et al. |
Sep 1991 |
|
Foreign Referenced Citations (4)
Number |
Date |
Country |
70 053 |
Jan 1983 |
EPX |
196 132 |
Oct 1986 |
EPX |
WO9316050 |
Aug 1983 |
WOX |
WO9400458 |
Jan 1994 |
WOX |