Amination of pyrido[3,2,1-jk]carbazol-6-ones

作者：Dang HV; Stadlbauer W^*

来源：Journal of Heterocyclic Chemistry, 2006, 43(1): 65-70.

DOI：10.1002/jhet.5570430110

Amination of 4-hydroxypyridocarbazolones 1 with aniline or benzylamine gave in good yields 4-amines 3. With piperidine in a sealed tube from 4-hydroxy- or 4-chloro-5-alkylpyridocarbazolones 1 or 4 ring opened 1-acylcarbazoles 5 were obtained. Only 4-hydroxy-5-phenyl-pyridocarbazolone 1d gave 4-amines 6. Reduction of 4-azidopyridocarbazolones 7 either by catalytic hydrogenation or in a 2-step synthesis via phosphazenes 8 gave 4-aminopyridocarbazolones 9. Amines 9 were also obtained from benzylamines 3 by catalytic debenzylation. A one step amination of 4-hydroxy-5-phenylpyridocarbazolone 1d via debenzylation to 9d was observed by reaction with benzylammonium chloride. At elevated temperatures the highly fused 6,13b-diazaindeno[1,2,3-hi]chrysenone 10 was formed from 1d.

• 出版日期2006-2