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method of preparation of the cetique cyclohexylgeranyla acid and some of its derivatives, pharmaceutical use
method of preparation of the cetique cyclohexylgeranyla acid and some of its derivatives, pharmaceutical use
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机译:西提克环己基香叶酸及其衍生物的制备方法,医药用途
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1420802 Substituted geranylacetic acids PRINCETON BIOMEDIX Inc 19 June 1973 [14 July 1972] 28940/73 Heading C2C The invention comprises substituted geranylacetic acids of the structure wherein R is selected from substituted and unsubstituted alkyl having from 1 to 10 carbon atoms, aryl, aralkyl, alkaryl, cycloalkenyl and substituted and unsubstituted cycloalkyl having from 5 to 8 carbon atoms in the ring; and RSP1/SP is selected from H, COOH and ON; provided that when R is cyclohexyl or cyclopentyl, RSP1/SP is COOH or CN and salts thereof. The substituted geranylacetic acids of the structure wherein R is as above, are prepared by a method comprising the steps of condensing a carbonyl compound selected from RSP11/SP=O and in which RSP11/SP and RSP111/SP are the divalent and trivalent derivatives of R with ethyl cyanoacetate to form a condensation product of the formula reducing said condensation product with sodium borohydride to form the cyanoacetate of the formula geranylating said cyanoacetate with a geranyl halide, hydrolysing the product of said geranylation step and decarboxylating the same to form said substituted geranylacetic acid. Cyclohexylgeranylacetic acid may be prepared by a method which comprises condensing citral with diethyl malonate to form a condensation product, reducing said condensation product with sodium borohydride to form diethyl 2- geranylmalonate; reacting this with sodium hydride and alkylating with cyclohexyl bromide to form diethyl 2-cyclohexyl-2-geranylmalonate which in turn is hydrolysed with potassium hydroxide, acidified with sulphuric acid and decarboxylated by heating at up to 160‹ C. Substituted geranylmalonic acids of the structure wherein R is as defined above, may be prepared by a method which comprises the steps of condensing a carbonyl compound selected from RSP11/SP=O and (wherein RSP11/SP and RSP111/SP are as above) with ethyl cyanoacetate to form a condensation product of the formula reducing said condensation product with sodium borohydride to form the cyanoacetate of formula geranylating this with a geranyl halide and hydrolysing the product to form said substituted geranylmalonic acid. The compounds of the invention are used for treating dermatological disorders.
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