Synthesis of substituted (oxazepine, Diazepine, tetrazde) via Schiff Bases for 2- Aminobenzo Thaizole Derivatives
Main Article Content
Abstract
This work includs synthesis of several Schiff bases by condensation of 6- methoxy – 2- amino benzothiazole with some aldehydes and ketones (2- hydroxyl benzaldehyde, 4- hydroxyl benzaldehyde, 4- N,N –dimethy amino acetophenone, benzophenone) to abtain schiff bases (1-5). These schiff bases were found to react with phthalate anhydride to give oxazepine derivatives (6-10) that were reacted with primary aromatic amines to give Diazepine derivatives (11-15). Besides, we prepared new tetrazole derivatives (16-20) from the reaction of the prepared Schiff bases with sodium azide in the prepared compounds that were characterized by physical properties, FT-IR and some of the 1H-NMR and 13C –NMR spectroscopy.
Article Details
How to Cite
1.
Synthesis of substituted (oxazepine, Diazepine, tetrazde) via Schiff Bases for 2- Aminobenzo Thaizole Derivatives. Baghdad Sci.J [Internet]. 2013 Sep. 1 [cited 2024 Nov. 19];10(3):736-48. Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/2586
Section
article
How to Cite
1.
Synthesis of substituted (oxazepine, Diazepine, tetrazde) via Schiff Bases for 2- Aminobenzo Thaizole Derivatives. Baghdad Sci.J [Internet]. 2013 Sep. 1 [cited 2024 Nov. 19];10(3):736-48. Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/2586