Synlett 2012(1): 93-96  
DOI: 10.1055/s-0031-1290109
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York

The Chemistry of α,β-Ditosyloxy Ketones: A New and Convenient Route to 4,5-Diarylisoxazoles from α,β-Chalcone Ditosylates

Raj Kamal*a, Deepak Sharmab, Deepak Wadhwaa, Om Prakasha
a Department of Chemistry, Kurukshetra University, Kurukshrtra 136119, Haryana, India
e-Mail: kamalraj_sharma@rediffmail.com;
b Govt. Post Graduate College, Ambala Cantt 133001, Haryana, India
Further Information

Publication History

Received 18 July 2011
Publication Date:
13 December 2011 (online)

Abstract

The reaction of α,β-chalcone ditosylates with hydroxyl­amine hydrochloride under suitable conditions leads to a 1,2-aryl shift, thereby providing a new route to 4,5-disubstituted isoxazoles.

    References and Notes

  • 1a Bickel CL. Phillips EA. Exeter NH. J. Am. Chem. Soc.  1950,  72:  349 
  • 1b Sharma TC. Patel H. Bokadia MM. Indian J. Chem.  1973,  11:  703 
  • 1c Elkasaby MA. Salem MA. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem.  1980,  19:  571 
  • 1d Khurana JM. Markap GC. Sahoo PK. Synthesis  1991,  827 
  • 1e Holla BS. Shridhara K. Chim. Acta Turc.  1992,  20:  161 
  • 1f Vijayshree N. Samuelson AG. Tetrahedron Lett.  1992,  33:  559 
  • 1g Saoudi A. Hamelin J. Benhaoua H. J. Chem. Res., Synop.  1996,  11:  491 
  • 1h Khurana JM. Seghal A. Synth. Commun.  1996,  26:  3791 
  • 1i Elba ME. Darwish AI. Hamada NM. Egypt. J. Chem.  1997,  40:  81 
  • 1j Elba ME. Darwish AI. Hamada NM. J. Indian Chem. Soc.  1997,  74:  202 
  • 1k Elba ME. Phosphorus, Sulfur Silicon Relat. Elem.  2000,  160:  233 
  • 1l Ranu BC. Janna R. J. Org. Chem.  2005,  70:  8621 
  • 2 Prakash O. Sharma D. Kamal R. Kumar R. Nair RR. Tetrahedron  2009,  65:  10175 
  • 3 Joshi MG. Wadodkar KN. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem.  1981,  20:  1090 
  • 4 Brough PA. Aherne W. Barril X. Borgognoni J. Boxall K. Cansfield JE. Cheung K.-MJ. Collins I. Davies NGM. Drysdale MJ. Dymock B. Eccles SA. Finch H. Fink A. Hayes A. Howes R. Hubbard RE. James K. Jordan AM. Lockie A. Martins V. Massey A. Matthews TP. McDonald E. Northfield CJ. Pearl LH. Prodromou C. Ray S. Raynaud FI. Roughley SD. Sharp SY. Surgenor A. Walmsley DL. Webb P. Wood M. Workman P. Wright L. J. Med. Chem.  2008,  51:  196 
  • 5 Habeeb AG. Rao PNP. Knaus EE. J. Med. Chem.  2001,  44:  2921 
  • 6 Kwon BM, Son KH, Han DC, Lee , S K, Shin KD, Jeon SB, and Oh JH. inventors; US Patent;  0131036. 
  • 7 Rebrovic L. Koser GF. J. Org. Chem.  1984,  49:  2462 
  • 8 Prakash O. Kumar R. Sharma D. Pannu K. Kamal R. Synlett  2007,  2189 
  • 10 Simons BK. Kallury RKMR. Bowie JH. Org. Mass Spectrom.  1969,  2:  739 
  • 12 Lang SA. Lin Y.-i. Comprehensive Heterocyclic Chemistry   Katritzky AR. Rees CW. Pergamon Press; Oxford: 1984.  p.4.16 
  • 13 Murthy MSR. Rao EV. Indian J. Chem.  1985,  24:  667 
  • 14 Subba GV. Rao KS. Curr. Sci.  1987,  56:  1280 
  • 15 Seishi TI. Hiroyuki Y. Yakugaku Zasshi  1959,  79:  467 
  • 16 Marques CS. Moura N. Burke AJ. Tetrahedron Lett.  2006,  47:  6049 
  • 17 E1-Sadany SK. Sharaf SM. Hamed EA. Fleishaur J. Darwish A.-I. Youssef AA. Egypt. J. Chem.  1991,  34:  401 
  • 18 Orloov VD. Kolos NN. Theni M. Yurr’eve E. Ivkov SM. Chem. Heterocycl. Compd. (Engl. Transl.)  1992,  28:  788 
  • 19 Kuroda C. Matsukuma T. Sci. Papers Inst. Phys. Chem. Research, Tokyo  1932,  18:  51 
  • 20 Weygand C. Stroblet F. Ber. Dtsch. Chem. Ges. B  1935,  68:  1839 
  • 21 Emerson WS. Patrick TM. J. Org. Chem.  1949,  790 
  • 22 Dannhardt G. Kiefer W. Kraemer G. Maehrlein S. Nowe U. Fiebich B. Eur. J. Med. Chem.  2000,  35:  499 
9

Experimental procedure used to prepare α,β-chalcone ditosylates 1: Prepared from the corresponding chalcones¹7-²² 3 using a procedure similar to that reported previously by our research group. Compounds 1a-c,g,i-j,l were previously reported, whereas 1d-f,h,k,m-o are novel compounds. Spectroscopic data of the latter compounds are given in the Supporting Information.

11

Experimental procedure used to prepare 4,5-diaryl-isoxazoles 4: A mixture of chalcone ditosylate (1a; 0.550 g, 0.001 mol), hydroxylamine hydrochloride (0.138 g, 0.002 mol) and sodium acetate (0.164 g, 0.002 mol) in EtOH (25 mL) was heated at reflux for approximately 3 h. The reaction mixture was then poured onto ice-cold water. The resulting mixture was extracted with CH2Cl2 (3 × 50 mL) and the combined organic extract was dried over anhydrous Na2SO4 and filtered. Evaporation of CH2Cl2 in vacuo gave the crude product, which was purified by column chromatography on silica gel (100-200 mesh; PE-EtOAc) to give pure pyrazole 4a (72%, 0.159 g). Other derivatives were prepared in a similar manner. Compounds 4e,g,h,j,k,m-o are novel. Spectroscopic data of these compounds are given in the Supporting Information.