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Abstract 2~IsO_propyl3,1,4_benzoxazjne (I) reacts with zary aromatic amine~ to give the Correspondmg 2— ~~lcarbamoyl)isobutrylmulideg (ii), and 2—(p—tolyl arnoyl)anjljne (III), And ~th hydra~jn~ hydrate and :c ~tEzylbydrazjne yielded the corre sp ending quinazolj~o~08 R~ ~), and (VI). The q’~nazolia~o~~ (Iv) reacts ~th ~ 4~zzaldehyde in presence of ethanol and gave the quina— C~i~ne Cv). Also the benzoxazone (I) reacts with ~ ~ffo2~lanthie hydrochloride and produced the hydro~r— 4k; jfij~ ~znazolinon~ (VII) in a good yield, Alcoholic ammonia formaynjde react with benzoxazone (I) and yielded ~(VIII) and quinazo1j~c~~ (Ix) 4~5 ~Øpectively. The latter exists actually in a lactani— ( aotira taur-omerjc oqui1ibrj~~ The reaction of benzoxazono I C) we~ 8~end~ to include reaction of toluene ui~der e ?~e4e1~r~tIs condition and phenylmagnesj~ bromide and renzfl m~nesjum chloride and yielded substituted benzo— ::enone (x), carbinol (xx) and substitutea desorybenzojji Also sodium azide/aoetic acid reaqts 4 r_;h benzoxaz~ie (z) to give tetrazole ( |