Intermediates for the preparation of lipoxin A
View Patent ↗This invention is directed to lipoxin A 4 analogs of the following formula (I) and (II): wherein R 1 , R 2 , R 3 , R 4 and R 5 are described herein. These analogs are useful in treating inflammatory and autoimmune disorders in humans. These analogs are also useful in treating pulmonary or respiratory tract inflammation in humans.
1. A compound of the following formula:
wherein,
R 5 is aryl (optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxy, halo, haloalkyl and haloalkoxy) or aralkyl (optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxy, halo, haloalkyl and haloalkoxy);
R 7 is alkyl, cycloalkyl, aryl, or aralkyl; and
R 10 is a straight or branched alkylene chain, a straight or branched alkenylene chain, a straight or branched alkynylene chain, or cycloalkylene;
as a single stereoisomer, a mixture of stereoisomers, or a racemic mixture of stereoisomers.
2. The compound according to claim 1 wherein
R 5 is aryl (optionally substituted by one or more substituents selected from the group consisting of alkyl, alkoxy, halo, and haloalkoxy);
R 7 is alkyl; and
R 10 is a straight or branched alkylene chain.
3. The compound according to claim 2 wherein R 7 is tert-butyl and R 10 is methylene.
4. The compound according to claim 3 wherein R 5 is optionally-substituted phenyl.
5. The compound according to claim 4 having the formula:
6. The compound tert-butyl 2-{[(4E,6E,10E)-(2S,3R,12S)-13-(4-fluorophenoxy)-2,3,12-trihydroxytrideca-4,6,10-trien-8-yn-1-yl]oxy}acetate, according to claim 5 .