首页> 外国专利> THE INDUSTRIAL METHOD FOR SYNTHESIS OF 17α-ACETOXY-11β- 4- (N, N-DIMETHYLAMINO) PHENYL -19-NORPREGNA-4,9-DIEN-3,20-DIONA AND NEW INTERMEDIATE CONNECTIONS RECEIVED UNITED SOURCE, UNITED SOURCE

THE INDUSTRIAL METHOD FOR SYNTHESIS OF 17α-ACETOXY-11β- 4- (N, N-DIMETHYLAMINO) PHENYL -19-NORPREGNA-4,9-DIEN-3,20-DIONA AND NEW INTERMEDIATE CONNECTIONS RECEIVED UNITED SOURCE, UNITED SOURCE

机译:合成17α-乙酰基11β-[4-(N,N-二甲基亚氨基)苯基] -19-NORPREGNA-4,9-DIEN-3,20-Diona的工业方法和新的中间连接方法接受统一来源,统一来源

摘要

The present invention relates to a new industrial method for the synthesis of unsolvated 17α-acetoxy-11β- [4- (N, N-dimethylamino) phenyl] -19-norpregna-4,9-diene-3,20-dione [CDB-2914] of the formula ( I), which is a strong antiprogestogen and antiglucocorticoid agent. The present invention also relates to compounds of formulas (VII) and (VIII) used as intermediates in the process. The method of the present invention is as follows: i) 3- (ethylenedioxy) estra-5 (10), 9 (11) -diene-17-one of formula (X) is reacted with potassium acetylide obtained in situ in dry tetrahydrofuran known by the method, ii) the obtained 3-ethylenedioxy) -17α-ethynyl-17β-hydroxy-estra-5 (10), 9 (11) -diene of the formula (IX) is reacted with phenylsulphenyl chloride in dichloromethane in the presence of triethylamine and acetic acid, iii ) the resulting mixture of isomers of 3- (ethylenedioxy) -21- (phenylsulfinyl) -19-norpregn-5 (10), 9 (11), 17 (20), 20-tetraene of formula (VIII) is first reacted with sodium methoxide in me anole, then with trimethylphosphite, iv) the obtained 3- (ethylenedioxy) -17α-hydroxy-20-methoxy-19-norpregn-5 (10), 9 (11), 20-triene of formula (VII) are reacted with hydrogen chloride in methanol, then v) the resulting 3- (ethylenedioxy) -17α-hydroxy-19-norpregn-5 (10), 9 (11) -diene-20-one of formula (VI) is reacted with ethylene glycol in dichloromethane in the presence of trimethyl orthoformate and p-toluenesulfonic acid by a known method, vi) the resulting 3,3,20,20-bis (ethylenedioxy) -17α-hydroxy-19-norpregn-5 (10), 9 (11) -diene of the formula (V) are reacted with hydrogen peroxide in a mixture of pyridine and dichloromethane in the presence of hexachloroacetone according to a known method, vii) the obtained 3,3,20,20-bis (ethylenedioxy) -17α-hydroxy-5,10-epoxy-19-norpregn-9 (11) -en of formula (IV) containing a mixture of 5α , 10α and 5β, β-epoxides of approximately 1: 1 are isolated from the solution and reacted with the Grignard reagent obtained
机译:本发明涉及一种合成未溶剂化的17α-乙酰氧基-11β-[4-(N,N-二甲基氨基)苯基] -19-降冰片烯-4,9-二烯-3,20-二酮[CDB]的新工业方法。 -2914]的式(I),它是强的抗孕激素和抗糖皮质激素药。本发明还涉及在该方法中用作中间体的式(VII)和(VIII)的化合物。本发明的方法如下:i)将式(X)的3-(亚乙二氧基)estra-5(10),9(11)-二烯-17-之一与在干燥的四氢呋喃中原位获得的乙炔化钾反应。通过该方法已知,ii)使所得的式(IX)的3-亚乙二氧基)-17α-乙炔基-17β-羟基-estra-5(10),9(11)-二烯与苯基磺酰氯在二氯甲烷中反应。 iii)三(乙二氧基)-21-(苯亚磺酰基)-19-norpregn-5(10),9(11),17(20),20-四烯的异构体的混合物式(VIII)首先与甲酸钠中的甲醇钠反应,然后与亚磷酸三甲酯反应,iv)得到的3-(乙二氧基)-17α-羟基-20-甲氧基-19-norpregn-5(10),9(11),使式(VII)的20-三烯与氯化氢在甲醇中反应,然后v)所得的3-(乙二氧基)-17α-羟基-19-norpregn-5(10),9(11)-二烯-20-使式(VI)的化合物与乙二醇在二氯甲烷中反应e通过已知方法存在原甲酸三甲酯和对甲苯磺酸,vi)所得3,3,20,20-双(乙二氧基)-17α-羟基-19-norpregn-5(10),9(11)-根据已知方法,在六氯丙酮存在下,使式(V)的二烯与吡啶和二氯甲烷的混合物中的过氧化氢反应,vii)获得的3,3,20,20-双(亚乙二氧基)-17α-羟基含有5α,10α和5β的混合物的式(IV)的-5,10-环氧-19-norpregn-9(11)-en,从溶液中分离出约1:1的β-环氧化合物,并与格氏试剂反应获得的试剂

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