Synthesis 2018; 50(24): 4982-4988
DOI: 10.1055/s-0037-1610239
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 1-Carboxamide-1,4-dihydropyridazines via Recycli­zation of Hydroxypyrrolines with Semicarbazides

Dmitrii A. Shabalin
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
,
Evgeniya E. Ivanova
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
,
Anton V. Kuzmin
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
b   Limnological Institute, Siberian Branch of the Russian Academy of Sciences, 3 Ulan-Batorskaya St, Irkutsk 664033, Russian Federation
,
Marina Yu. Dvorko
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
,
Elena Yu. Schmidt
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
,
Boris A. Trofimov*
a   A. E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch of the Russian Academy of Sciences, 1 Favorsky St, Irkutsk 664033, Russian Federation   Email: boris_trofimov@irioch.irk.ru
› Author Affiliations
The reported study was funded by RFBR according to the research project No. 18-33-00089. The spectral data were obtained with the equipment of the Baikal Analytical Center for collective use SB RAS.
Further Information

Publication History

Received: 28 May 2018

Accepted after revision: 19 July 2018

Publication Date:
22 August 2018 (online)


Abstract

Recyclization of available 5-hydroxypyrrolines with semicarbazide and its analogues has been studied. As a result, rare 1,4-dihydropyridazines with carboxamide function at the N-1 atom have been synthesized in up to 88% isolated yields.

Supporting Information

 
  • References

    • 1a Triggle DJ. Cell. Mol. Neurobiol. 2003; 23: 293
    • 1b Welsch ME. Snyder SA. Stockwell BR. Curr. Opin. Chem. Biol. 2010; 14: 347
  • 2 Chiou GC. Y. Yao QS. Okawara T. J. Ocul. Pharmacol. 1994; 10: 577
    • 3a Frankowiak G. Meyer H. Bossert F. Heise A. Kazda S. Stoepel K. Towart R. Wehinger E. Patent US4348395, 1982
    • 3b Loev B. Jones H. Shroff JR. Patent US4435395, 1984
    • 3c Vogel A. Patent US 4491581, 1985
  • 4 Shang X. Song X. Faller C. Lai R. Li H. Cerny R. Niu W. Guo J. Chem. Sci. 2017; 8: 1141
  • 5 Vázquez A. Dzijak R. Dračínský M. Rampmaier R. Siegl SJ. Vrabel M. Angew. Chem. Int. Ed. 2017; 56: 1334
  • 6 Koçak R. Yıldız D. Bozkaya U. Daştan A. Bozdemir ÖA. Tetrahedron Lett. 2017; 58: 2981
  • 7 Bagge RE. Mauldin TC. Boday DJ. Kobilka BM. Loy DA. Chem. Mater. 2017; 29: 7953
    • 8a Seitz G. Kämpchen T. Arch. Pharm. 1975; 308: 237
    • 8b Adembri G. Chimichi S. Nesi R. Scotton M. J. Chem. Soc., Perkin Trans. 1 1977; 1020
    • 8c Regitz M. Welter W. Hartmann A. Chem. Ber. 1979; 112: 2509
    • 8d Heydt H. Busch K.-H. Regitz M. Liebigs Ann. Chem. 1980; 590
    • 8e Abdelmoniem AM. Abdelhamid IA. Curr. Org. Chem. 2016; 20: 1512
    • 8f Mata S. González MJ. González J. López LA. Vicente R. Chem. Eur. J. 2017; 23: 1013
    • 9a Shabalin DA. Dvorko MYu. Schmidt EYu. Protsuk NI. Trofimov BA. Tetrahedron Lett. 2016; 57: 3156
    • 9b Shabalin DA. Dvorko MYu. Schmidt EYu. Ushakov IA. Trofimov BA. Tetrahedron 2016; 72: 6661
  • 10 Shabalin DA. Dvorko MYu. Zolotareva EE. Ushakov IA. Vashchenko AV. Schmidt EYu. Trofimov BA. Eur. J. Org. Chem. 2017; 4004
    • 11a Zabicky J. In The Chemistry of Amides . J. Wiley & Sons; London: 1970
    • 11b Pace V. Holzer W. Olofsson B. Adv. Synth. Catal. 2014; 356: 3697
  • 12 Ghose AK. Viswanadhan VN. Wendoloski JJ. J. Comb. Chem. 1999; 1: 55
  • 13 Nagarajan K. David J. Shah RK. J. Med. Chem. 1976; 19: 508
    • 14a Hamad A.-SS. Hashem AI. Acta Chim. Slov. 2001; 48: 431
    • 14b Hamad A.-SS. Hashem AI. J. Heterocycl. Chem. 2002; 39: 1325
  • 15 Attanasi OA. Berretta S. De Crescentini L. Favi G. Filippone P. Giorgi G. Mantellini F. Tetrahedron 2010; 66: 6832
  • 16 Becke AD. J. Chem. Phys. 1993; 98: 5648
  • 17 Stephens PJ. Devlin FJ. Chabalowski CF. Frisch MJ. J. Phys. Chem. 1994; 98: 11623
  • 18 Tomasi J. Mennucci M. Cances E. J. Mol. Struct. (Theochem) 1999; 464: 211
  • 19 Frisch MJ. Trucks GW. Schlegel HB. Scuseria GE. Robb MA. Cheeseman JR. Scalmani G. Barone V. Mennucci B. Petersson GA. Nakatsuji H. Caricato M. Li X. Hratchian HP. Izmaylov AF. Bloino J. Zheng G. Sonnenberg JL. Hada M. Ehara M. Toyota K. Fukuda R. Hasegawa J. Ishida M. Nakajima T. Honda Y. Kitao O. Nakai H. Vreven T. Montgomery JrJ. A. Peralta JE. Ogliaro F. Bearpark M. Heyd JJ. Brothers E. Kudin KN. Staroverov VN. Kobayashi R. Normand J. Raghavachari K. Rendell A. Burant JC. Iyengar SS. Tomasi J. Cossi M. Rega N. Millam NJ. Klene M. Knox JE. Cross JB. Bakken V. Adamo C. Jaramillo J. Gomperts R. Stratmann RE. Yazyev O. Austin AJ. Cammi R. Pomelli C. Ochterski JW. Martin RL. Morokuma K. Zakrzewski VG. Voth GA. Salvador P. Dannenberg JJ. Dapprich S. Daniels AD. Farkas O. Foresman JB. Ortiz JV. Cioslowski J. Fox DJ. Gaussian 09, Revision A.02 . Gaussian Inc; Wallingford, CT: 2009