Synthesis 2003(16): 2559-2563  
DOI: 10.1055/s-2003-42414
PAPER
© Georg Thieme Verlag Stuttgart · New York

A Novel Route to 1,2,3-Thiadiazole, 1,3,4-Thiadiazine, and 1,2,5-Triazepine Derivatives

Barbara Zaleska*a, Bartosz Trzewika, Jacek Grochowskib, Paweł Serdab
a Department of Organic Chemistry, Jagiellonian University, ul. Romana Ingardena 3, 30-060 Kraków, Poland
Fax: 48(12)6340515; e-Mail: zaleska@chemia.uj.edu.pl;
b Regional Laboratory of Physicochemical Analyses and Structural Research, ul. Romana Ingardena 3, 30-060 Kraków, Poland
Further Information

Publication History

Received 3 July 2003
Publication Date:
29 September 2003 (online)

Abstract

New convenient methods for the synthesis of 1,2,3-thiadiazole, 1,3,4-thiadiazine, and 1,2,5-triazepine derivatives are reported. In the heterocyclization process, the reactivity of 1-thia-4-aza-1,3-butadiene system of syn-2-phenylhydrazono-3-oxothiobutanoic acid anilides was exploited.

    References

  • 1a Cyraski MK. Krygowski TM. Katritzky AR. von Schleyer P. J. Org. Chem.  2002,  67:  1333 
  • 1b Glossman-Mitnik D. THEOCHEM  2001,  549:  285 
  • 2a Shafiee A. Jalilian AR. Rezaei M. J. Heterocycl. Chem.  2000,  37:  1325 
  • 2b Naidu AV. Dave MA. Asian. J. Chem.  2000,  687 
  • 3a Abramov MA. Dehaen W. D’hooge B. Petrov ML. Smeet S. Toppet S. Voets M. Tetrahedron  2000,  56:  3933 
  • 3b Hameurlaine A. Abramov MA. Dehaen W. Tetrahedron Lett.  2002,  43:  1015 
  • 4 Zhang Z, Yan J, Leung D, Wang S, Costello PC, and Sanghera J. inventors; US  6420400.  ; Chem. Abstr. 2002, 137, 93758p
  • 5 Schwarz M, Page P, Pomel V, Quattropani A, and Thomas RJ. inventors; PCT Int. Appl. WO  02102799.  ; Chem. Abstr. 2003, 138, 55968v
  • 6a Shin KJ. Koo KD. Yoo KH. Kang YK. Park WS. Kim DJ. Bioorg. Med. Chem. Lett.  2001,  11:  2397 
  • 6b Yamamoto H. Terasawa T. Nakamura A. Kawabata K. Takasugi H. Tanaka H. Matsumoto S. Matsumoto Y. Tawara S. Bioorg. Med. Chem.  2001,  9:  465 
  • 7a Fujii K, Hatano K, and Yoshida J. inventors; Jpn. Kokai Tokkyo Koho JP 2001  335570.  ; Chem. Abstr. 2002, 136, 20074g
  • 7b Lindell S, Dickhaut J, Jakobi H, Tiebes J, Jans D, Thoenessen M.-T, and Waibel JM. inventors; Eur. Pat. Appl. EP  1236727.  ; Chem. Abstr. 2002, 137, 201314b
  • 7c Uchikurohashi T, Tashima T, Yamamoto Y, Otsuka T, Yamaguchi R, and Imano T. inventors; Jpn. Kokai Tokkyo Koho JP 2002  114612.  ; Chem. Abstr. 2002, 136, 305521n
  • 8a Shibamoto S. J. Chem. Soc., Perkin Trans. 1  1992,  3233 
  • 8b Bianchi M. Butti A. Rossi S. Tetrahedron  1974,  30:  2765 
  • 9 Zaleska B. Bazanek T. Socha R. Karelus M. Grochowski J. Serda P. J. Org. Chem.  2002,  67:  4526 
  • 10 Zaleska B. Socha R. Monatsh. Chem.  2000,  131:  1151 
  • 11 Zaleska B. Socha R. Ciechanowicz-Rutkowska M. Pilati T. Monatsh. Chem.  2000,  131:  1158 
  • 12 Zaleska B. Socha R. Grochowski J. Serda P. Szneler E. J. Org. Chem.  2003,  68:  2334 
  • 13 Zaleska B. Cie¿ D. Haas A. Synth. Commun.  1996,  26:  4165 
14

Compound 2a crystallizes in the monoclinic system. See experimental for details of X-ray structure determination. The structural data have been deposited at the Cambridge Crystallographic Data Centre under the reference number CCDC 209483.