首页> 外国专利> SUBSTITUTED (R)-3-(4-METHYLCARBAMOYL-3-FLUOROPHENYLAMINO)-TETRAHYDRO-FURAN-3-ENE CARBOXYLIC ACIDS AND ESTERS THEREOF, METHOD FOR PRODUCTION AND USE THEREOF

SUBSTITUTED (R)-3-(4-METHYLCARBAMOYL-3-FLUOROPHENYLAMINO)-TETRAHYDRO-FURAN-3-ENE CARBOXYLIC ACIDS AND ESTERS THEREOF, METHOD FOR PRODUCTION AND USE THEREOF

机译:取代的(R)-3-(4-甲基氨基甲酰基-3-氟苯甲酰氨基)-四氢-呋喃-3-烯羧酸及其酯,制备方法和用途

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to novel substituted 3-(4-methylcarbamoyl-3-fluorophenylamino)tetrahydrofuran-3-ene carboxylic acid or esters thereof of general formula 1 and stereoisomers. The compounds of formula 1 are intermediate products in synthesis of androgen receptor inhibitors of formula A1, A2, A3, which are of interest as anticancer drugs. The invention also relates to methods of producing compounds of formula 1 and compounds of formulae A1, A2, A3. In general formula 1 R1=H, C1-C4alkyl; R2=H, CH2OCH2CH2Si(CH3)3. The method of producing compounds of formula (1) involves reacting compounds of general formula 2 with compounds 3(1) or 3(2) in dimethylformamide, K2CO3 while simultaneously adding copper iodide, water and triethylamine to the reaction mass. 2: By reacting compounds of formula 1, obtained using said method, with 4-isothiocyanato-2-trifluoromethylbenzonitrile in a mixture of dimethyl sulphoxide and ethyl acetate in ratio of 1:2 and at high temperature, compounds A1, A2, A3, whose structure is given in the claim, are obtained, respectively.;EFFECT: use of novel intermediate products improves output and stereoselectivity of the method of producing compounds A1, A2, A3.;4 cl, 6 ex
机译:发明领域本发明涉及新型的通式1的取代的3-(4-甲基氨基甲酰基-3-氟苯基氨基)四氢呋喃-3-烯羧酸或其酯和立体异构体。式1的化合物是合成式A1,A2,A3的雄激素受体抑制剂的中间产物,其作为抗癌药是有意义的。本发明还涉及制备式1的化合物和式A1,A2,A3的化合物的方法。在一般公式1中 R 1 = H,C 1 -C 4 烷基; R 2 = H,CH 2 OCH 2 CH 2 Si(CH 3 3 。制备式(1)的化合物的方法包括使通式2的化合物与化合物3(1)或3(2)在二甲基甲酰胺,K 2 CO 3 中反应。同时向反应物料中加入碘化铜,水和三乙胺。 2:<图像文件=“ 00000019.GIF” he =“ 49” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 145” />通过使用上述方法获得的式1化合物与4-isothiocyanatoato-比例为1:2的二甲基亚砜和乙酸乙酯的混合物中的2-三氟甲基苯甲腈,在高温下,分别获得化合物A1,A2,A3,其结构在权利要求中给出;效果:使用新型中间体产品提高了化合物A1,A2,A3的制备方法的输出和立体选择性; 4 cl,6 ex

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