Synthesis of 2‐Chirally Substituted 3,3′‐Biquinazoline‐4,4′‐diones

A facile route for the synthesis of 2‐substituted biquinazolinones incorporating a chiral center into one of their lateral appendage, via condensation of 4 H ‐3,1‐benzoxazin‐4‐one with 3‐amino‐2 S ‐substituted‐quinazolin‐4‐ones, is described. The methodology is straightforward and does not require chromatographic purification at any stage. The products are obtained in good yields as mixture of diastereoisomers, which can be enriched with the major diastereoisomer by simple recrystallization. The functional groups in the lateral chain can be easily modified allowing the synthesis of a variety of 3,3′‐biquinazoline‐4,4′‐diones. The synthesis of symmetrically 2,2′ chirally disubstituted biquinazolinones via acylation/dehydration sequence of bisanthraniloyl hydrazine is also described.