## Abstract For Abstract see ChemInform Abstract in Full Text.
Synthesis, characterization and spectral studies of various newer 4-benzyloxy-1H-indole-2-carboxylic acid (arylidene)-hydrazides
✍ Scribed by Asheesh Kumar Jain; Pradeep Kumar Gupta; Kumaran Ganesan; Ambuja Pande; Deepak Pardasani; Ramesh Chandra Malhotra
- Book ID
- 102344864
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 111 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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✦ Synopsis
Abstract
4‐Benzyloxyindole‐2‐carboxylic acid hydrazide reacts with aromatic and heterocyclic aldehydes in alcoholic medium in refluxing conditions to give 4‐benzyloxy‐1__H__‐indole‐2‐carboxylic acid (arylidene)‐hydrazides, important synthetic intermediates for the synthesis of a newer class of pharmacologically active compounds. We describe here the synthesis of various 4‐benzyloxy‐1__H__‐indole‐2‐carboxylic acid (arylidene)‐hydrazides by conventional as well as microwave irradiation techniques. The structures of these compounds have been confirmed by spectroscopic techniques (FTIR, NMR and MS). Some of the interesting features of the electron impact mass spectral fragmentation pattern of these compounds are also discussed.
📜 SIMILAR VOLUMES
## Abstract Ketene generated from acetyl chloride or chloroacetyl chloride adds on indolyl Schiff's base double bond to afford 1‐butyl‐3‐substituted‐4‐(2‐aryl‐1__H__‐indol‐3‐yl)‐2‐azetidinones in THF. The reaction proceeds stereospecifically via concerted __trans__ [2+2] cycloaddition. The synthesi