Reactions of Morphine Derivatives with Phenyliodo(III)Diacetate (PIDA) Synthesis of New Morphine Analogues+,++

Author(s):

S. Garadnay, P. Herczegh, S. Makleit, T. Friedmann, P. Riba and S. Furst   Pages 621 - 626 ( 6 )

Abstract:

The reactions of morphine and its derivatives with phenyliodo(III)diacetate (PIDA) have been studied. This methodology has not been introduced to morphine alkaloids, despite the fact that such a strategy would ensure dearomatization of the electrophilic aromatic ring of morphine derivatives leading to nucleophilic ortho-quinoidal structures with potential pharmacological interest. The products, formed in regio- and diastereoselective or diastereospecific reactions, carry mixed-acetal or 1,3-dioxolane moieties. At low concentrations 6a has µ-opioid agonist character but in higher concentrations showed a non receptorial antagonist effect on isolated mouse vas deferens.

Keywords:

Morphine,Phenyliodo(III)Diacetate,Morphine Analogues,GPI,Mouse vas deferens MVD

Affiliation:

, , , , , Dept. of Pharmacology, Semmelweis University of Medicine, Budapest, Hungary

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