N-heterocyclic-N-(4-piperidyl)amides and pharmaceutical compositions and methods employing such compounds
AssigneeThe BOC Group, Inc.
InventorsJerome R. Bagley, H. Kenneth Spencer
Life of this patent
Estimating the term…
Abstract
N-heterocyclic-4-piperidyl-amides as analgesics and antagonists of opioids with respect to such undesirable side effects as respiratory depression. Exemplary compounds have the formula ##STR1## in which formula R is a heterocyclic group, and R.sup.1 is a furanyl, thienyl, or lower alkoxy lower alkyl group, and R.sup.2 is a lower alkyl phenyl group.
Claims28
A compound of the formula ##STR24## optically active isomeric forms thereof, or pharmaceutically acceptable acid addition salts thereof, in which formula:
- R is pyrrolyl, pyrazyl, pyridyl, pyrimidyl, or triazolyl, all of which may be unsubstituted or substituted wherein the substituents are selected from the group consisting of halogen, lower alkyl, lower alkoxy, halogenated lower alkyl, lower alkylthio or combinations thereof;
- R.sup.1 is a furanyl or thienyl or a lower alkoxy lower alkyl of 2 to 6 carbon atoms;
- and R.sup.2 is a phenyl lower alkyl.
A method for causing in a mammal the reversal of one or more actions of narcotic analgesics or anesthetics, said actions including respiratory depression, comprising administering to said mammal an antagonistically effective amount of N-piperidyl-N-heterocyclic substituted furamide, thienylamide or lower alkoxy lower alkylamide and derivatives thereof, optically isomeric forms thereof, or pharmaceutically acceptable acid addition salts thereof, comprising administering to such mammal an antagonistically effective amount selectively reversing respiratory depression but not analgesia.
A method for producing analgesia or selective reversal of the actions of opiate analgesics, including respiratory depression, in a mammal comprising administering to such mammal an analgesically or antagonistically effective amount of a compound of the formula ##STR25## optically active isomeric forms thereof, or pharmaceutically acceptable acid addition salts thereof, in which formula R is pyrrolyl, pyrazyl, pyridyl, pyridmidyl, triazolyl, all of which may be unsubstituted or substituted wherein the substituents are selected from the group consisting of halogen, lower alkyl, lower alkoxy, halogenated lower alkyl, lower alkylthio or combinations thereof;
- R.sup.1 is a furanyl or a thienyl or a lower alkoxy lower alkyl of 2 to 6 carbon atoms;
- and R.sup.2 is a phenyl lower alkyl.
A narcotic antagonistic or analgesic composition comprising a non-toxic pharmaceutically acceptable carrier and an analgesically or antagonistically effective amount of a compound of the formula ##STR26## optically active isomeric forms thereof, or pharmaceutically acceptable acid addition salts thereof, in which formula R is pyrrolyl, pyrazyl, pyridyl, pyridmidyl or triazolyl, all of which may be unsubstituted or substituted by one or more substituents selected from the group consisting of halogen, lower alkyl, lower alkoxy, halogenated lower alkyl, lower alkylthio, or combinations thereof. R.sup.1 is a furanyl or a thienyl a lower alkoxy lower alkyl of 2 to 6 carbon atoms;
- and R.sup.2 is a phenyl lower alkyl.
Dependencies are inferred from the claim text.