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PROCESS FOR OBTAINING NEW P-BIPHENYL ESTERS OF 15-SUBSTITUTED OMEGA-PENTANO PROSTAGLANDINS

机译:获得15个取代的美加五角ENT前列腺素的新对苯二甲酸酯的方法

摘要

1456511 Prostaglandins PFIZER Inc 1 Nov 1973 [8 Nov 1972] 50889/73 Heading C2C The invention comprises prostaglandins of the formula I and the C 15 epimers thereof, wherein A is Ar(CH 2 ) n - or -(CH 2 ) m -ORSP2/SP, W is a single bond or cis double bond, Z is a single bond or trans double bond; m is oxo or n is 0 to 5 when Z is a single bond, or n is 1 to 5 when Z is a trans double bond; m is 2 or 3; RSP2/SP is C 1-4 alkyl; Ar is - or #-furyl, - or #-thienyl, - or #-naphthyl, 3,4-dimethoxyphenyl, 3,4-methylenedioxyphenyl, 3,4,5-trimethoxyphenyl or phenyl optionally monosubstituted by halogen, trifluoromethyl, phenyl, C 1-4 alkyl or C 1-4 alkoxy; R 1 is p-biphenylyl, R is H or C 1-4 alkyl, X and Y together form a single bond or X is H and Y is alpha-hydroxy, with the proviso that when X and Y form a single bond m is oxo; and compounds of the Formulµ II, III and VI or and their C 15 epimers, wherein m is oxo or Compounds of Formula I above are obtained by esterifying the corresponding acids of Formula I in which RSP1/SP and X are hydrogen and Y is alpha-hydroxy with p-phenylphenol, and if desired, dehydrating the resulting compounds in which m is oxo and Y is alpha-hydroxy. The esters of the prostaglandin E and F series may also be obtained by hydrolysing the corresponding 11,15-bis-(tetrahydropyranyl) ethers of Formula VI above which are obtained by reacting compounds of the Formula VII with compounds of the formula and if desired, oxidizing and/or hydrogenating the resulting compounds of formula VI above in which m is Compounds of Formula II and III above are obtained by reacting compounds of formula VII above with compounds of the formula and if desired, oxidizing and/or hydrogenating the resulting compounds of Formula II above. Biphenylyl 9,15 - dioxo - 11 - hydroxy - 17- phenyl - 18,19,20 - trinor - cis - 5, trans - 13- prostadienoate is obtained by oxidizing biphenylyl 9 - oxo - 11,15# - dihydroxy - 17- phenyl - 18,19,20 - trinor - cis - 5, trans - 13- prostadienoate with manganese dioxide. Pharmaceutical compositions, suitable for oral, intravaginal, intraamniotically, intravenous or intranasal administration, contain the above esters of Formula I together with suitable carriers or diluents. The compound possess similar pharmacological properties to those of the naturally occurring prostaglandins. Reference has been directed by the Comptroller to Specifications 1,386,146, 1,345,934 and 1,324,737.
机译:1456511前列腺素PFIZER Inc 1973年11月1日[1972年11月8日] 50889/73标题C2C本发明包括式I的前列腺素及其C 15差向异构体,其中A为Ar(CH 2)n-或-(CH 2)m- OR 2 ,W为单键或顺式双键,Z为单键或反式双键;当Z为单键时,m为氧代或n为0至5,或当Z为反式双键时,n为1至5。 m为2或3; R 2 为C 1-4烷基; Ar为-或#-呋喃基,-或#-噻吩基,-或#-萘基,3,4-二甲氧基苯基,3,4-亚甲基二氧基苯基,3,4,5-三甲氧基苯基或任选被卤素,三氟甲基,苯基取代的苯基, C 1-4烷基或C 1-4烷氧基; R 1是对联苯基,R是H或C 1-4烷基,X和Y一起形成一个单键或X是H并且Y是一个α-羟基,条件是当X和Y形成一个单键时m是氧代以及其中m是氧代的式II,III和VI的化合物或其C 15差向异构体或以上式I的化合物是通过酯化其中R 1 和X的相应的式I的酸而获得的氢为氢,Y为对苯酚的α-羟基,如果需要的话,将所得的化合物脱水,其中m为氧代且Y为α-羟基。前列腺素E和F系列的酯还可以通过水解相应的上述式VI的11,15-双-(四氢吡喃基)醚来获得,其通过使式VII的化合物与该式的化合物反应获得,并且如果需要,氧化和/或氢化上面的式Ⅵ化合物,其中m是上面的式Ⅱ和Ⅲ的化合物是通过使上面的式VII的化合物与通式的化合物反应得到的,如果需要的话,氧化和/或氢化的式Ⅱ的化合物可以得到。上面的公式II。通过氧化联苯基9-羰基-11,15#-二羟基-17-获得联苯基9,15-二恶基-11-羟基-17-苯基-18,19,20-trinor-顺-5,反式-13-前列二烯酸酯。苯基-18,19,20-trinor-顺-5,反式-13-前列二烯酸酯,含二氧化锰。适用于口服,阴道内,羊膜内,静脉内或鼻内给药的药物组合物包含上述式I的酯以及合适的载体或稀释剂。该化合物具有与天然前列腺素相似的药理特性。主计长已对规格1,386,146、1,345,934和1,324,737进行了参考。

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