

SYNTHESIS AND ANTIHERPETIC ACTIVITY OF NOVEL PURINE CONJUGATES WITH 7,8-DIFLUORO-3-METHYL-3,4-DIHYDRO-2H-1,4-BENZOXAZINE

Abstract
A method for the synthesis of novel purine conjugates with 7,8-difluoro-3-methyl-3,4-dihydro-2H-1,4-benzoxazine containing fragments of ω-amino acids with different lengths of the polymethylene chain as a linker has been developed. It was found in experiments in vitro that the obtained compounds are active against the herpes simplex virus type 1, including the acyclovir-resistant strain.
Keywords
ω-amino acids; 6-chloropurine; 7,8-difluoro-3-methyl-3,4-dihydro-2H-1,4-benzoxazine; antiviral activity; herpes simplex virus type 1.
Latvian Institute of Organic Synthesis - Aizkraukles iela, 21, Riga, LV-1006, Latvia - hgs@osi.lv