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Antineoplastic agents 389. New syntheses of the combretastatin A-4 prodrug.
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1998
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Antineoplastic Agents 389Bioorganic ChemistryPharmaceutical ChemistryPhosphate Ester ProdrugMolecular PharmacologyMedicinal ChemistryBiosynthesisAnti-cancer AgentBiochemistryBioconjugationDrug DevelopmentNatural Product SynthesisPharmacologyBiomolecular EngineeringCombretastatin A-4Benzyl EstersPolymer-drug ConjugateNatural SciencesMedicineDrug Discovery
Combretastatin A-4 (1) as the phosphate ester prodrug (3d) is a potent antineoplastic and antiangiogenesis substance and is in advanced preclinical development. For the purpose of improving the phosphorylation synthetic sequence from combretastatin A-4, new routes were investigated. The phosphorylation step was found to be considerably improved using in situ-generated dibenzyl chlorophosphite. Cleavage of the benzyl esters employing a trimethylchlorosilane/sodium iodide procedure, followed by treatment with sodium methoxide, led to the water-soluble prodrug (3d) in high yield.