SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF ETHYL 3-(N-ARYLIMINOMETHYL)-5-CHLORO-1H-INDOLE-2-CARBOXYLATE | ||
| Zagazig Journal of Pharmaceutical Sciences | ||
| Article 5, Volume 16, Issue 2, December 2007, Pages 35-38 PDF (1.15 M) | ||
| Document Type: Original Article | ||
| DOI: 10.21608/zjps.2007.169387 | ||
| Authors | ||
| Mohamed Said* 1; Nagat Ghareb1; Adel El-Gendy2 | ||
| 1Organic Chemistry Department, Faculty of Pharmacy, Suez Canal University, Ismailia, Egypt. | ||
| 2Organic Chemistry Department, Faculty of Pharmacy, Cairo University, Cairo, Egypt. | ||
| Abstract | ||
| Condensation of 4-chlorophenylhydrazine (1) with ethyl pyruvate led to the formation of ethy1 pyruvate 4- chlorophenyl thydrazone (2) Fischer Indolization of (2) gave ethyl 5-chloro-1H-indole-2-carboxylate (3). Vilsmeier-Hacck formylation of (3) gave ethyl 5-chloro-3-formyl-1H-indole-2-carboxylate (4). The reaction of (4) with substituted anilines led to the formation of ethytl 3-(N-aryliminomethyl)-5-chloro-1H-indole-2-carboxylate (5-10). Structures of the new compounds were confirmed by both analytical and spectral data (IR, NMR and MS). Antimicrobial screening was also performed. | ||
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