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WJPR Citation
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| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
MICROWAVE MEDIATED SYNTHESIS OF PHARMACOLOGICAL ACTIVE SUBSTITUTED DERIVATIVES OF 2-(4/-PHENOTHIAZINYL PYRAZOLYL) PYRROLES
Dr. Meghasham N. Narule, Dr. Mahesh K. Gaidhane, Dr. Pravin K. Gaidhane
Abstract Phenothiazines belong to an important class of heterocyclic compounds known for their pharmaceutical properties. Phenothiazine core is the active component in sedatives, tranquilizers, antituberculotics or bactericides. Phenothiazines are electron donor compounds with a low oxidation potential and they can form easily radical-cations.Lately phenothiazine has become very popular in material science or in biochemistry as marker for proteins and DNA. 2- [4/-hydroxyl benz-1/-(propene-1//-one)] Pyrrole (2) on treatment with primary amine gives 2-[biphenyl amine-1/-(propane-1//-one)] pyrrole (3) which react with sulphur and iodine affording substituted 2- [phenothiazinyl-8/-(propane-1//-one)] pyrrole (4a-j) which undergoes cyclization with NH2.NH2H2O and Substituted 2-(4/-phenothiazinyl pyrazolyl) pyrrole (5a-j) is obtained. The structure products were characterized by elemental analysis and spectral data. Keywords: Pyrrole, Phenothiazinyl pyrazolyl, Pharmacological activity, Microwave method. [Full Text Article] [Download Certificate] |
