12 H -Benzo[1,3]oxazolo[2,3-b]quinazolin-12-imine ( 5a ), 9-chloro-12 H -benzo[1,3]oxazolo[2,3-b]quinazolin-12-imine ( 5b ), 2,3-dihydro-5 H -[1,3]oxazolo[2,3-b]quinazolin-5-imine ( 5c ), 2,3-dihydro-3,3-dimethyl-5 H -[1,3]oxazolo[2,3-b]quinazolin-5-imine ( 5d ) and 3,4--dihydro-2 H ,6 H -[1,3]oxazino[2,3-b]quinazolin-6-imine ( 5e ) weresynthesized in a one-pot reaction of N-(2-cyanophenyl)chloromethanimidoyl chloride ( 1 )with 2-aminophenols, 2-aminoethanol, and 3-aminopropanol in the presence of a base. Thecourse of the reaction was controlled by the temperature and the amount of base used. N -(2-Cyanophenyl)-(2-hydroxyanilino)methanimidoyl chloride ( 3a ), 2-chloro-3-(2-hydroxy-phenyl)-3,4-dihydroquinazolin-4-imine ( 4a ) and 6-imino-2 H , 3 H , 4 H , 6 H , 11 H -1,3-oxazino[2,3-b]-5-quinazolinium chloride ( 6 ) were identified as intermediates of the one-pot process. Keywords: N -(2-cyanophenyl)chloromethanimidoyl chloride, 1,3-oxazolo[2,3-b]-quinazoline, 1,3-oxazino[2,3-b]quinazoline, methanimidoyl chloride, fused quinazolines