首页> 外国专利> METHOD FOR SYNTHESISING DISODIUM SALT OF DEXAMETHASONE 21-PHOSPHATE APPLIED FOR TREATING PATIENTS WITH CORONAVIRUS INFECTION (COVID-19)

METHOD FOR SYNTHESISING DISODIUM SALT OF DEXAMETHASONE 21-PHOSPHATE APPLIED FOR TREATING PATIENTS WITH CORONAVIRUS INFECTION (COVID-19)

机译:用于合成地塞米松21-磷酸二钠盐的方法,适用于治疗冠状病毒感染患者(Covid-19)

摘要

FIELD: chemistry.;SUBSTANCE: present invention relates to a method for synthesising disodium salt of dexamethasone (11,17βα-dihydroxy-9α-fluoro-16α-methyl-21-(phosphonooxy)pregna-1,4-diene-3,20-dione) 21-phosphate by the formula (I) - a corticosteroid medicinal product exhibiting a desensitising, antishock, immunosuppressive, antiallergic, anti-inflammatory effect. The compound by the formula I is produced from dexamethasone (11β,17α,21-trihydroxy-9α-fluoro-16α-methylpregna-1,4-diene-3,20-dione) by the formula (II) by means of a reaction with pyrophosphoryl chloride taken at the rate of no less than 1.0 mol per 1.0 mol of the compound II, in the environment of a cyclic ether, followed by hydrolysis of the resulting 21-phosphate dexamethasone dichloro-derivative, removal of steroid impurities from the aqueous medium by the method of liquid-phase extraction using chlorinated hydrocarbon, extraction of the formed dexamethasone (11β,17α-dihydroxy-9α-fluoro-16α-methyl-21-(phosphonooxy)pregna-1,4-diene-3,20-dione) 21-phosphate by the formula (III) from the aqueous medium by the method of solid-phase extraction at room temperature using non-ionogenic polymers selected from Macronet MN-200, Macronet MN-202, AmberLite XAD-4, AmberLite XAD-16, desorption thereof by a mixture of chlorinated hydrocarbon and aliphatic alcohol, and processing of 21-phosphate dexamethasone with sodium alcoholate in the environment of the corresponding aliphatic alcohol, wherein no less than 1.94 moles of sodium alcoholate is taken per 1 mol of the compound III.;EFFECT: proposed method provides a possibility of synthesising a target product of the appropriate quality while ensuring a molar yield of at least 90%.; ; ;10 cl, 3 ex
机译:田地:化学。物质:本发明涉及一种合成地塞米松二钠盐的方法(11,17βα-二羟基-9α-氟-16α-甲基-21-(膦酰氧基)PREGNA-1,4-二烯-3,20 - 二酮)通过式(I)的21-磷酸 - 一种皮质类固醇药品,其表现出脱敏,反锁,免疫抑制,抗炎症,抗炎作用。通过反应,通过式(II)由式(11β,17α,21-三羟基-9α-氟-16α-甲基甲基甲基预浸甲基-1,4-二烯-3,20-二酮)由式(11β,17α,21-三羟基-16α-甲基预浸甲基-1,4-二烯-3,20-二酮)制备。在环醚的环境中以每1.0摩尔的化合物II的速率不小于1.0mol的溶解率,然后将所得的21磷酸含量的二氯衍生物水解,从水性中除去类固醇杂质通过氯化烃的液相萃取方法,提取形成的地塞米松(11β,17α-二羟基-9α-氟-16α-甲基-21-(膦酰氧基)PREGNA-1,4-二烯-3,20-通过使用选自MARRONET MN-200,MACRONET MN-202,Amberlite Xad-4,Amberlite Xad-4,Amberlite Xad-4,氨氯酸盐XAD-4,Amberlite Xad-4的非离子化聚合物在室温下由水性相萃取方法21-磷酸盐由水性相萃取的方法。 -16,通过氯化烃和脂族醇的混合物来解吸,以及21-磷酸的加工在相应的脂族醇的环境中,用钠醇钠溶液,其中每1摩尔的化合物III采用不小于1.94摩尔钠醇。;效果:提出的方法提供了合成适当质量的目标产品的可能性确保至少90%的摩尔收益率。 ; ; 10 cl,3 ex

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