Esters of 2-adamantanone oxime are prepared and are disclosed as possessing anti-inflammatory activity and antiviral activity against murine hepatitis virus.
Description
INTRODUCTION AND BACKGROUND The present invention provides a novel class of 2-adamantanone oxime esters that possess anti-inflammatory activity. While certain imino-2-adamantanes are known (Biochem. Pharmacol 31, 1693, (1982); C.A. 94, 46371r (1981); Ger. 2651083; C.A. 89 129241w, (1978)), one of which was reported to have psychotropic activity, the oxime esters of the present invention have not been reported. THE INVENTION The present invention provides a novel class of esters of 2-adamantanone oxime of Formula I below: ##STR1## wherein R represents lower alkyl, lower alkenyl, aryl, aralkyl and aralkenyl wherein the aryl groups may bear substituents for hydrogen, such as, for instance, nitrile, nitro, halo and alkoxy. The compounds of the present invention can be conveniently prepared by reacting 2-adamantanone oxime with sodium hydride followed by the addition of an appropriate acid chloride. The following example is cited to illustrate the invention. It is not intended to limit it in any manner.
EXAMPLE 1 0-(Phenylacetyl)-2-Adamantanone Oxime 2-Adamantanone oxime (10.0 g, 0.061 mol) was added to a suspension of sodium hydride (2.93 g, 0.122 mol) in 60 mol tetrahydrofuran and the reaction mixture was refluxed for 5 hours. Then, phenylacetyl chloride (9.43 g, 0.061 mol) was added slowly and the reaction mixture was refluxed for 6 hours. After cooling, chloroform was added and the inorganic precipitate was filtered off. The organic solution was evaporated to dryness leaving a crude oxime ester derivative (9 g) which was recrystallized from cyclohexane, providing purified 0-(phenylacetyl)-2-adamantanone oxime melting between 74.degree. and 80.degree. C. The technique of Example 1 was employed to prepare a series of related compounds as identified in the Table below using the appropriate acid chloride and a suitable recrystallization solvent (as indicated). TABLE______________________________________ recryst'n.Example R mp, .degree.C. solvent______________________________________2 CH.sub.3 108-110 iso-PrOH3 C.sub.6 H.sub.4 CN4 144-146 iso-PrOH4 C.sub.6 H.sub.4 NO.sub.24 160-161 iso-PrOH5 C.sub.6 H.sub.4 NO.sub.23 123-126 iso-PrOH ##STR2## 84-85 iso-PrOH7 ##STR3## 70-73 petr. ether8 CHCHCH.sub.3 76-80 iso-PrOH9 ##STR4## 129-131 iso-PrOH10 ##STR5## 136-139 iso-PrOH______________________________________ The compounds of this invention have displayed biological activity, particularly as anti-inflammatory agents as indicated by results of the Carrageenan-induced rat paw edema assay. In addition, the compound of Example 3 has exhibited antiviral activity against murine hepatitis virus. Many equivalent modifications of the above invention will become apparent to those skilled in the art without a departure from the inventive concept.
Claims
1. The compounds ##STR6## wherein R is a member of the class of lower alky, lower alkenyl, aryl, aralkyl and aralkenyl wherein the aryl groups may bear substituents for hydrogen selected from the group consisting of nitrile, nitro, halo and alkoxy.
2. The compound of claim 1 wherein R is ##STR7##
3. The compound of claim 1 wherein R is CH.sub.3.
4. The compound of claim 1 wherein R is C.sub.6 H.sub.4 CN--4.
5. The compound of claim 1 wherein R is C.sub.6 H.sub.4 NO.sub.2 --4.
6. The compound of claim 1 wherein R is C.sub.6 H.sub.4 NO.sub.2 --3.
7. The compound of claim 1 wherein R is ##STR8##
8. The compound of claim 1 wherein R is ##STR9##
9. The compound of claim 1 wherein R is CH.dbd.CHCH.sub.3.
10. The compound of claim 1 wherein R is ##STR10##
11. The compound of claim 1 wherein R is ##STR11##
Patent Grant
4486601
