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Benzodiazines nucleophilic substitution

Reactions of benzodiazines show no exceptional features compared with the simple diazines. Reactivity towards electrophiles is less than in quinoline and isoquinoline. If S Ar reactions take place, they lead to substitution of the benzene ring. As a rule, nucleophilic substitution of benzodiazines occur in the diazine ring, particularly if substituted by halogen. The quinazoline system displays C-4 regioselectivity, e.g. in the reactions of 2,4-dichloroquinazoline with amines or alcohols ... [Pg.431]


See other pages where Benzodiazines nucleophilic substitution is mentioned: [Pg.4]   
See also in sourсe #XX -- [ Pg.369 , Pg.370 , Pg.371 , Pg.372 , Pg.373 , Pg.374 , Pg.375 , Pg.376 ]

See also in sourсe #XX -- [ Pg.369 , Pg.370 , Pg.371 , Pg.372 , Pg.373 , Pg.374 , Pg.375 , Pg.376 ]

See also in sourсe #XX -- [ Pg.369 , Pg.370 , Pg.371 , Pg.372 , Pg.373 , Pg.374 , Pg.375 , Pg.376 ]




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Benzodiazine

Benzodiazines

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