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method of preparation of the cetique cyclohexylgeranyla acid and some of its derivatives, pharmaceutical use

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

摘要

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.
机译:1420802取代的香叶菊酸PRINCETON BIOMEDIX Inc 1973年6月19日[1972年7月14日]标题C2C本发明包括具有以下结构的取代的香叶菊酸,其中R选自具有1至10个碳原子的取代和未取代的烷基,芳基,芳烷基,环中具有5至8个碳原子的烷芳基,环烯基以及取代和未取代的环烷基; R 1 选自H,COOH和ON。前提是当R是环己基或环戊基时,R 1 是COOH或CN及其盐。具有R的上述结构的取代的香叶乳酸是通过以下方法制备的:该方法包括缩合选自R 11 = O且其中R 11 和R 111 是R与氰基乙酸乙酯的二价和三价衍生物,形成下式的缩合产物:将所述缩合产物与硼氢化钠还原,形成下式为香叶酸的氰基乙酸盐,将所述氰基乙酸盐与香叶基基团酰化。卤化物,水解所述香叶酰化步骤的产物并将其脱羧以形成所述取代的香叶酸。环己基香叶酸可通过以下方法制备:将柠檬醛与丙二酸二乙酯缩合以形成缩合产物,用硼氢化钠还原所述缩合产物以形成2-香叶基丙二酸二乙酯。使之与氢化钠反应,再与环己基溴化物烷基化,形成2-环己基-2-香叶基丙二酸二乙酯,然后用氢氧化钾水解,用硫酸酸化,并在最高160°C的温度下加热脱羧。结构取代的香叶基丙二酸其中R如上定义的,可以通过包括以下步骤的方法制备:使选自R 11 = O和(其中R 11 和R < SP> 111 如上)与氰基乙酸乙酯形成下式的缩合产物,将所述缩合产物与硼氢化钠还原,形成下式为香叶酸的氰基乙酸盐,将其与香叶基卤化,然后水解该产物,形成所述取代的香叶基丙二酸。酸。本发明的化合物用于治疗皮肤病。

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