Palladium chloride derivative, structure

Scheme 9.23 Proposed structure for the dinuclear palladium complex derived from a chiral propargyl chloride.

By NMR analyses, prenylpalladium complex 17, derived from palladium chloride 5 and prenylmagnesium chloride in situ, was confirmed to take a a-allyl form with the C-Pd bond at the less substituted carbon atom (Scheme 9.4) [21]. This result strongly supports the proposed structure of 14 and its carboxylation at y-position. 

The synthesis of this salt started with the enantiomerically pure 1,2-diamine 106, that was converted into the corresponding thiourea derivative 107 (Scheme 12). Exposure of the thiourea 107 to oxalyl chloride in toluene at 60 °C cleanly afforded the desired imidazolinium chloride 108. These two salts were used to produce new palladium and nickel carbene complexes. The structure of both palladium carbene complexes 96a and 96b has been elucidated by X-ray diffraction <2005CEJ1833>. 

A series of pyrido[2,3-rf pyrimidine-2,4-diones bearing substituents at C-5 and/or C-6 were synthesized using palladium-catalyzed coupling of uracil derivative 417 with vinyl substrates or allyl ethers to give the regioisomeric mixtures of 418/419 and 420/421, respectively. The ratio of the isomeric structures was dependent on the substituent R. In the case of the reaction with -butyl vinyl ether, only the product 419 was obtained. However, the reactions with acrylonitrile, ethyl acrylate, 2-trifluoromethylstyrene, and 3-nitrostyrene afforded only 418. Also, reaction with allyl phenyl ether gave only 420. The key intermediate 417 was prepared by the reaction of 6-amino-l-methyluracil with DMF-DMA (DMA = dimethylacetamide), followed by N-benzylation with benzyl chloride and vinyl iodination with iV-iodosuccinimide (NIS) (Scheme 15) <2001BML611>. 

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