The title process comprises a method which does not employ 9,10-unsatd. precursors. Thus, 5-cyano-10,11-dihydro-5H-dibenz[b,f]azepine was brominated and the product hydroxylated to give 5-cyano-10 hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine which was converted to the title compd
5-Cyano-10-hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine, processes for its preparation and for its conversion into 5-carbamoyl-10-oxo-10,11-dihydro-5H-dibenz[b,f]azepine or into 5-carbamoyl-5H-dibenz[b,f]azepine
CITTERIO, ATTILIO;
2001-01-01
Abstract
The title process comprises a method which does not employ 9,10-unsatd. precursors. Thus, 5-cyano-10,11-dihydro-5H-dibenz[b,f]azepine was brominated and the product hydroxylated to give 5-cyano-10 hydroxy-10,11-dihydro-5H-dibenz[b,f]azepine which was converted to the title compdFile in questo prodotto:
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