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Volume 2006
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10.3390/M517
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Short Note

Synthesis of 3-[(Z)-5-Amino-1, 3, 3-trimethyl cyclohexyl methylimino]-1, 3-dihydroindol-2-one as a novel Schiff base

by
Ramakrishna Reddy K.
and
Mahendra K. N.
*
Department of Chemistry, Central College Campus, Bangalore University, Bangalore-560001, India
*
Author to whom correspondence should be addressed.
Molbank 2006, 2006(6), M517; https://doi.org/10.3390/M517
Submission received: 21 July 2006 / Accepted: 20 October 2006 / Published: 1 December 2006
Versions Notes

Isatin (1H-indole-2,3-dione) was first obtained by Erdman and Laurent in 1841 as a product from the oxidation of indigo by nitric and chromic acids [1]. The synthetic versatility of isatin has led to the extensive use of this compound in organic synthesis. In nature, isatin is found in plants of the genus Isatis [2], in Calanthe discolor LINDL [3]. Isatin is the biologically active chemical produced by an Altermones sp. Strain inhabiting the surface of embryos of the cardiean shrimp Palaemon macrodectylus, which protect them from the pathogenic fungus Lagenidium callinectes [4]. Schiff bases of isatin were reported to possess interesting biological activities such as anti-HIV [5,6,7], anticonvulsant [8], antibacterial [9,10,11], antiprotozoal [12,13], antifungal [14,15,16], antiviral [17,18,19], anthelminthic [20,21], antidepressant [22] anti-inflammatory and antitumour [23] activities. In view of the potent biological activities, we decided to synthesize a new isatin Schiff base by the condensation of isatin with isophoronediamine (IPDA). The Schiff bases of isatin have also been used as a ligand for complexation with various metal ions [24].The biological activities, epoxy curing studies of the new Schiff base and its chelating behaviour with various metal ions is under progress.
Ethanolic solutions of isatin (1) (0.01mol, 1.479) in 50 ml and isophoronediamine (2) (5-amino-1,3,3- trimethyl-cyclohexanemethylamine)(0.01mol, 1.8ml, 1.79g) in 50 ml were mixed and refluxed for about 2 hours. The reaction mixture was evaporated to a small volume and left to cool. The resulting Schiff base (3) ligand precipitated on cooling and then was filtered off, washed with ethanol and recrystallised from ethanol. The purity of the Schiff base ligand was monitored on TLC using eluants 1:1 ethyl acetate and petroleum ether and separated by column chromatography (Yield =90%).
Molbank 2006 m517 i001
Melting point: 117°C.
Elemental analysis: Calculated for C18H25N3O: C, 72.14; H, 8.35; N, 14.03. Found: C, 71.95; H, 8.33; N, 13.98.
IR (KBr, cm-1): 1618.6 (C=N), 1714.6 (C=O), 3239.9 (N-H).
MS (ESI, m/z): 299 [M+].
1H-NMR (400MHz, DMSO-d6): 10.5 (1H, s) 7.5-6.8 (5H, m), 2.4(2H, m), 1.5-0.65(18H, m).
13C-NMR (400MHz, DMSO-d6):23.5; 28.1; 35.3; 43.5; 45.5; 47.1; 49.2; 50.2; 57.2; 111.0; 119.9; 120.9; 122.3; 131.0; 132.0; 142.3; 168.8.

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3

References

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  3. Yoshikawa, M.; Murakami, T.; Kishi, A.; Sakurama, T.; Matsuda, H.; Nomura, M.; Matsuda, H.; Kubo, M. Chem. Pharm. Bull. 1998, 46, 886. [PubMed]
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  24. Rama Krishna Reddy, K.; Madhusudan Reddy, K; Mahendra, K.N. Ind.J.of Chem 2006, 45A, 377.

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MDPI and ACS Style

K., R.R.; N., M.K. Synthesis of 3-[(Z)-5-Amino-1, 3, 3-trimethyl cyclohexyl methylimino]-1, 3-dihydroindol-2-one as a novel Schiff base. Molbank 2006, 2006, M517. https://doi.org/10.3390/M517

AMA Style

K. RR, N. MK. Synthesis of 3-[(Z)-5-Amino-1, 3, 3-trimethyl cyclohexyl methylimino]-1, 3-dihydroindol-2-one as a novel Schiff base. Molbank. 2006; 2006(6):M517. https://doi.org/10.3390/M517

Chicago/Turabian Style

K., Ramakrishna Reddy, and Mahendra K. N. 2006. "Synthesis of 3-[(Z)-5-Amino-1, 3, 3-trimethyl cyclohexyl methylimino]-1, 3-dihydroindol-2-one as a novel Schiff base" Molbank 2006, no. 6: M517. https://doi.org/10.3390/M517

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