## Abstract The synthesis of N‐[5‐(2‐phenoxyphenyl)‐1, 3, 4‐oxadiazole‐2‐yl]‐N′‐phenylurea derivatives is reported. The structures of these compounds are supported by their IR, ^1^H‐NMR and mass spectra. Conformational analysis and superimposition of energy minima conformers of these compounds on L
Synthesis and CNS Activity of N,N-Disubstituted 1-(Aminomethyl)-5-alkyl-3-(aryloxyacetylhydrazono)indolin-2-ones
✍ Scribed by Rajesh Agarwal; Shobha Misra; Rajiv K. Satsangi; Shiva S. Tiwari
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- English
- Weight
- 245 KB
- Volume
- 315
- Category
- Article
- ISSN
- 0365-6233
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✦ Synopsis
Abstract
Isatin and 5‐methylisatin were condensed with various aryloxyacetylhydrazides to furnish the 3‐(aryloxyacetylhydrazono)‐5‐alkylindolin‐2‐ones 1–4. When 1–4 were subjected to Mannich reaction, the N,N‐disubstituted 1‐(aminomethyl)‐5‐alkyl‐3‐(aryloxyacetylhydrazono)indolin‐2‐ones 5–8 were obtained. The compounds were CNS active and relatively non‐toxic (albino mice).
📜 SIMILAR VOLUMES
Regioselective functionalization of 2,4,5,6-tetrachloro-1, 3-dicyanobenzene (TCDCB) by nucleophilic substitution of the chlorine at C(4) with L-Ala, L-Phe or L-Pro, followed by amide-bond formation to lipophilic amines containing strong pi-donor group, and by final introduction of the spacer 3-amino