US 5,183,818 AGranted

Arylalkylether and arylalkylthioether inhibitors of lipoxygenase enzyme activity

AssigneeAbbott Laboratories

InventorsDee W. Brooks, Andrew O. Stewart, Jonathan G. Martin

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Abstract

The present invention provides compounds having the structure Y-Het-[Q.sub.1 ]-X-[Q.sub.2 ]-Z which inhibit the catalytic action of lipoxygenase enzymes, particularly 5-lipoxygenase, and thereby reduce the biosynthesis of leukotrienes B.sub.4, C.sub.4, D.sub.4, and E.sub.4. In the generic formula given above, X is oxygen or sulfur and Het is a heteroaryl group selected from the group consisting of furyl, thienyl, 2-, 3-, and 4-pyridyl, 2- and 3-benzo[b]furyl, 2- and 3-benzo[b]thienyl and thienothienyl. Y is one or two substituents independently selected from hydrogen, hydroxy, halogen, cyano, alkyl, haloalkyl, alkoxy, alkylthio, alkoxyaryl), alkylthioaryl, arylalkoxy, arylalkylthio, aryloxy, arylthio, alkylamido, cycloalkyl, alkanoyl, alkoxycarbonyl, amino, alkylamino, dialkylamino, and the following groups wherein R, at each occurrence, is independently selected from hydrogen and alkyl of from one to six carbon atoms: --CRROR, --NRC(O)R, --NRC(O)OR, and --C(O)NRR. The group Q.sub.1 is absent or is divalent alkylene of from one to six carbon atoms, and Q.sub.2 is divalent alkylene from from two to ten carbon atoms. The group Z is N(OR.sub.1)COR.sub.2 where R.sub.1 is selected from hydrogen or a pharmaceutically suitable salt. R.sub.2 is selected from hydrogen; alkyl; cycloalkyl; amino; alkylamino, optionally substituted by hydroxyl, halogen, alkoxy or carboxyl; dialkylamino in which the alkyl groups are independently are optionally substituted by hydroxyl, halogen, alkoxy or carboxyl; cycloalkylamino; 2-hydroxyethylamino; N-morpholino; N-thiomorpholino; N-piperazine; N'-alkyl-N-piperazine and cyclopropylmethylamino.

A compound of the formula ##STR8## or a pharmaceutically acceptable salt thereof wherein X is oxygen or sulfur;

Y is one or two substituents independently selected from the group consisting of
hydrogen,
hydroxy,
halogen,
cyano,
alkyl of from one to six carbon atoms,
halogenated alkyl of from one to six carbon atoms,
alkoxy of from one to six carbon atoms,
alkylthio of from one to six carbon atoms,
alkoxy(carbocyclic aryl) in which the alkoxy portion contains from one to six carbon atoms,
alkylthio(carbocyclic aryl) in which the alkylthio portion contains from one to six carbon atoms,
(carbocyclic aryl)alkoxy in which the alkoxy portion contains from one to six carbon atoms,
(carbocyclic aryl)alkylthio in which the alkylthio portion contains from one to six carbon atoms,
(carbocyclic aryl)oxy,
(carbocyclic aryl)thio,
alkylamido of from one to six carbon atoms,
cycloalkyl of from three to eight carbon atoms,
alkanoyl of from one to six carbon atoms,
alkoxycarbonyl,
amino,
alkylamino of from one to six carbon atoms,
dialkylamino in which the two alkyl groups are independently selected from the group consisting of alkyl of from one to six carbon atoms,
--CRROR, --NRC(O)R, --NRC(O)OR, and --C(O)NRR wherein R, at each occurrence, is independently selected from hydrogen and alkyl of from one to six carbon atoms;
Q.sub.1 is divalent alkylene of from one to six carbon atoms;
Q.sub.2 is divalent alkylene from two to ten carbon atoms;
and
Z is N(OR.sub.1)COR.sub.2 wherein
R.sub.1 is selected from hydrogen or a pharmaceutically suitable salt, and
R.sub.2 is selected from the group consisting of
amino,
alkylamino of from one to six carbon atoms in which the alkyl group is optionally substituted by
hydroxyl,
halogen,
alkoxy, or
carboxyl,
dialkylamino in which the alkyl groups are independently selected from one to six carbon atoms and in which the alkyl groups are optionally independently substituted by
hydroxyl,
halogen,
alkoxy, or
carboxyl,
cycloalkylamino of from three to six carbon atoms, 2-hydroxyethylamino,
N-morpholino,
N-thiomorpholino,
N-piperazino,
N'-alkyl-N-piperazino, and
cyclopropylmethylamino.

43 more elements

Abstract

Claims7