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filingDate 1973-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1975-11-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1414047-A
titleOfInvention Ursolic acid derivatives
abstract 1414047 Ursolic acid derivatives BIOREX LABORATORIES Ltd 11 March 1974 [15 March 1973] 12427/73 Heading C2U The invention comprises compounds of formula wherein either (i) R<SP>1</SP> is an acyl radical of a polycarboxylic acid, and R<SP>11</SP> is OH (compounds Ia), or (ii) R<SP>1</SP> is H or an acyl radical of a mono- or polycarboxylic acid and R<SP>11</SP> is NR<SP>2</SP>R<SP>3</SP> where R<SP>2</SP> and R<SP>3</SP> are each H, an aliphatic radical of at least 3 carbon atoms or a cycloaliphatic or aromatic radical, or NR<SP>2</SP>R<SP>3</SP> is a heterocyclic radical optionally with further hetero atoms and/or substituents (compounds Ib); and the non- toxic salts of those compounds having at least one free carboxy group and/or at least one basic nitrogen atom. Compounds Ia are prepared by esterification of ursolic acid, and compounds Ib by reaction of an ursolic acid halide or 3-acylate thereof with R<SP>2</SP>R<SP>3</SP>NH. The inventive compounds are interconvertible by salification, desalification, and hydrolysis of 3-acyloxy. An acid chloride is prepared from ursolic acid acetate by the action of thionyl chloride. Oral and parenteral antiinflammatory compositions comprise a compound of the invention and a carrier.
priorityDate 1973-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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