Microwave-Assisted Synthesis of 3,1-Benzoxazin-2-ones from 3-Hydroxyoxindoles

Abstract

A general protocol for the synthesis of 3,1-benzoxazin-2-ones 18 from 3-hydroxyoxindoles 16 in a two steps sequence through phenylsuccinates or phenylpropionates 17 is described.Best reaction conditions for ring opening of 16 to succinates or propionates 17 were achieved using alcohol/silica gel, while cyclization of 17 to benzoxazinones 18 was easily done with HCl/alcohol.It was also found that 17 and 18 can be transesterified using HCl/alcohol.Most transformations were carried out by traditional heating and by microwave (MW) irradiation to accelerate reaction rates.N H O CO 2 Me NH 2 CO 2 Me N CO 2 Me MeOH H + CO 2 Me