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Asymmetric Synthesis of a New Monocyclic β-Lactam as a potential biological active compound

Department of Chemistry, College of Sciences, Shiraz University, Shiraz 71454, Iran
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Molbank 2005, 2005(4), M439; https://doi.org/10.3390/M439
Received: 2 June 2005 / Accepted: 22 September 2005 / Published: 1 October 2005
Keywords: Schiff base; asymmetric Staudinger reaction; [2+2] cycloaddition; monocyclic β-lactam Schiff base; asymmetric Staudinger reaction; [2+2] cycloaddition; monocyclic β-lactam
The asymmetric synthesis of monocyclic β-lactams belong to five categories: a) asymmetric induction from the imine component; b) asymmetric induction from the ketene component; c) double stereodifferentiating cycloadditions; d) carbacephem intermediates and e) 2-oxaisocephems and 2-isocephems. The asymmetric induction in the reaction of achiral ketenes with chiral imines has been effected from imines derived from chiral aldehydes and achiral amines and also from imines derived from chiral amines and achiral aldehydes[1,2,3,4,5,6]. Hashimoto and his coworkers have used chiral imines derived from erythro 2-methoxy-1,2-diphenylethylamine and aromatic aldehydes to prepare β-lactams in good yields with high diastereoselectivity [7]. Recently high levels of asymmetric induction has also been reported for monocyclic β-lactam formation [8,9]. Thus, we decided to synthesize a diastereoselective monocyclic β-lactam using the asymmetric induction by the chiral imine component and achiral ketene.
Treatment of S- (-)-tyrosine ethyl ester hydrochloride with 2-hydroxybenzaldehyde (salicylaldehyde) in the presence of triethylamine in dry benzene afforded Schiff base 1 as a yellow crystal. This chiral Schiff base was then transformed into the monocyclic β-lactam 2 bytreatment with achiral ketene which was prepared in situ from phthaloylglycyl chloride and triethylamine in dry methylene chloride.
Molbank 2005 m439 i001
To the cold solution of mixture of Schiff base 1 (3.13 g, 10.00 mmol) and phthaloylglycyl chloride (2.37 g, 10.00 mmol) in dry methylene chloride (30 ml/g of phthaloyl), was added slowly triethylamine (1.31 g, 13.00 mmol) in methylene chloride (10 ml/g of the base). The reaction mixture was stirred at room temperature for 24 hours. The formation of new product was confirmed by the presence of β-lactam carbonyl group at 1780 cm-1 in its IR spectrum. Then it was washed with water (3×30 ml). The organic layer was separated and dried (Na2SO4), filtered and the solvent was evaporated under reduced pressure. The crude β-lactam 2 was recrystalized from ether-hexane (3.13 g, 61%).
This [2+2] cycloaddition (Staudinger reaction) afforded the cis stereoisomer. The coupling costant for H3 and H4 was 6.19 Hz which is consistent with this kind of geometry. The other stereoisomer was not detected in TLC and NMR. Its biological activities such as antibacterial, antifungal, antiproliferative are under study.
Melting point: 158-160°C.
IR(KBr, cm-1): 1725; 1775 (Phthalimido CO); 1740 (CO2Et); 1784 (β-lactam CO); 3180-3300 (OH).
1H-NMR (250MHz, CDCl3): δ= 1.09-1.14 (3H, t, CH3); 3.11-3.20 (1H, t, CHCO2Et); 4.10-4.32 (4H, m, PhCH2, OCH2); 4.40-4.54 (1H, d, J=6.19 Hz, H4); 4.61-4.88 (1H, d, J=6.19, H3); 6.99-7.92 (12H, m, ArH).
MS (m/z, %): 500 (M+, 3.6%); 499 (M+ -1, 3.9%); 174 (PhthCH2CH2, 100.00%).

Supplementary materials

Supplementary File 1Supplementary File 2Supplementary File 3

Acknowledgment

The authors thank the Research Council of Shiraz University for financial support (Grant No. 83-GR-SC-31 and 84-GR-SC-23 ).

References

  1. Jarrahpour, A. A.; Shekarriz, M.; Taslimi, A. Molecules 2004, 9, 29.Jarrahpour, A. A.; Shekarriz, M.; Taslimi, A. Molecules 2004, 9, 939.
  2. Palomo, C.; Aizpurua, J. M.; Ganboa, I.; Oiarbide, M. Eur. J. Org. Chem. 1999, 3223.
  3. Palomo, C.; Aizpurua, J. M.; Ganboa, I.; Oiarbide, M. Amino Acids 1999, 16, 321. [PubMed]
  4. Ojima, I.; Chen, H. J. C.; Qiu, X. Tetrahedron 1988, 44(17), 5307.
  5. Van der Steen, F. H.; Van Koten, G. Tetrahedron 1991, 47, 7503.
  6. Georg, G. I.; Ravikumar, V. T. The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; WCH: New York, 1993; p. 295. [Google Scholar]
  7. Hashimoto, Y.; Ogasawara, T.; Hayashi, M.; Saigo, K. Heterocycles 2000, 52, 1001.
  8. Arunkumar, N.; Keyan, W.; Ramamurthy, V.; Scheffer, J. R.; Brain, P. Org. Lett. 2002, 4, 1443.
  9. France, S.; Wack, H.; Hafez, A. M.; Taggi, A. E.; Witsil, D. R.; Lectka, T. Org. Lett. 2002, 4, 1603. [PubMed]
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