PART I: NOVEL QUINOXALINE DERIVATIVES OF BIOLOGICAL INTEREST | ||||
Bulletin of Pharmaceutical Sciences Assiut University | ||||
Article 15, Volume 24, Issue 2, December 2001, Page 135-144 PDF (525.58 K) | ||||
Document Type: Original Article | ||||
DOI: 10.21608/bfsa.2001.65967 | ||||
![]() | ||||
Authors | ||||
M. M. Badran1; S. Botros1; A. A. El-Gendy1; N. A. Abdou1; H. El-Assi1; A. Salem2 | ||||
1Departments of 'Organic Chemistry | ||||
2Pharmacology, Faculty of Pharmacy, Cairo University, Cairo 11562, Egypt | ||||
Abstract | ||||
2-Substituted amino-Bi-tl-pyrazotyliquinoxalines 4-11 wereprepared by reacting 2-chloro- 3-hydrazinoquinoxaline 1 with 1,3-dicarbonyl compounds followed by treatment of the resulting 2-chloro-3-(1-pyrazolyl)quinoxlines 2,3 with the proper 2 ° amine. Reacting 1 with pyruvic acid or its ethyl ester afforded the corresponding hydrazone. Upon treating the hydrazone 15 with POCl3, the corresponding [1,2 ,4Jtriazino[4 ,3-a] quinoxallne 17 was achieved. Further, a series of 4-(piperazinyl) tetrazolojl ,5-a]quinoxalines 19-24 was prepared by reacting 1 with nitrous acid followed by treatment of the resulting 4-d,lorotetrazolo[l ,5-a]quinoxalines 18 with ]substituted piperazlnes. Biological testing of some of the prepared compounds revealed that these compounds may have antidepressant activity and compound 4 has the most pronounced effect | ||||
Statistics Article View: 126 PDF Download: 61 |
||||