Synthesis 2013; 45(3): 334-340
DOI: 10.1055/s-0032-1317945
paper
© Georg Thieme Verlag Stuttgart · New York

Selective Synthesis of Cyano-Functionalized 2-Aryl-4H-chromenes and 2-Amino-4H-chromene-3-carbonitriles by Catalyst-Tuned Reactions of 2-Hydroxychalcones with 2-Substituted Acetonitriles

Guodong Yin*
Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, P. R. of China   Fax: +86(714)6515602   Email: gdyin@hbnu.edu.cn
,
Houqiang Shi
Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, P. R. of China   Fax: +86(714)6515602   Email: gdyin@hbnu.edu.cn
,
Liqianyun Xu
Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, P. R. of China   Fax: +86(714)6515602   Email: gdyin@hbnu.edu.cn
,
Xianhong Wei
Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, P. R. of China   Fax: +86(714)6515602   Email: gdyin@hbnu.edu.cn
,
Qing Tao
Hubei Key Laboratory of Pollutant Analysis and Reuse Technology, College of Chemistry and Environmental Engineering, Hubei Normal University, Huangshi 435002, P. R. of China   Fax: +86(714)6515602   Email: gdyin@hbnu.edu.cn
› Author Affiliations
Further Information

Publication History

Received: 24 October 2012

Accepted after revision: 03 December 2012

Publication Date:
03 January 2013 (online)


Abstract

A selective synthesis of 4H-chromenes by the reactions of 2-hydroxychalcone derivatives with acetonitriles substituted with electron-withdrawing groups is described. Under catalyst-free conditions, the reactions give cyano-functionalized 2-aryl-4H-chromenes, whereas in the presence of sodium bicarbonate, 2-amino-4H-chromene-3-carbonitriles are obtained in excellent yields.

Supporting Information

 
  • References

    • 1a Patil SA, Wang J, Li XC. S, Chen JJ, Jones TS, Hosni-Ahmed A, Patil R, Seibel WL, Li W, Miller DD. Bioorg. Med. Chem. Lett. 2012; 22: 4458
    • 1b Khoshneviszadeh M, Edraki N, Miri R, Foroumadi A, Hemmateenejad B. Chem. Biol. Drug Des. 2012; 79: 442
  • 2 Anderson DR, Hegde S, Reinhard E, Gomez L, Vernier WF, Lee L, Liu S, Sambandam A, Snider PA, Masih L. Bioorg. Med. Chem. Lett. 2005; 15: 1587
    • 3a Skommer J, Wlodkowic D, Mättö M, Eray M, Pelkonen J. Leuk. Res. 2006; 30: 322
    • 3b Wang JL, Liu DX, Zhang ZJ, Shan S, Han XB, Srinivasula SM, Croce CM, Alnemri ES, Huang ZW. Proc. Natl. Acad. Sci. U.S.A. 2000; 97: 7124
    • 4a Costa M, Areias F, Abrunhosa L, Venâncio A, Proença F. J. Org. Chem. 2008; 73: 1954
    • 4b Proença F, Costa M. Green Chem. 2008; 10: 995
    • 4c Elinson MN, Ilovaisky AI, Merkulova VM, Belyakov PA, Chizhov AO, Nikishin GI. Tetrahedron 2010; 66: 4043
    • 4d Kumaravel K, Vasuki G. Green Chem. 2009; 11: 1945
    • 4e Gyuris M, Madácsi R, Puskás LG, Tóth GK, Wölfling J, Kanizsai I. Eur. J. Org. Chem. 2011; 848
    • 4f Du ZY, Siau WY, Wang J. Tetrahedron Lett. 2011; 52: 6137
    • 4g Gupta AK, Kumari K, Singh N, Raghuvanshi DS, Singh KN. Tetrahedron Lett. 2012; 53: 650
    • 5a Kolla SR, Lee YR. Tetrahedron 2012; 68: 226
    • 5b Murthy SN, Madhav B, Reddy VP, Nageswar YV. D. Tetrahedron Lett. 2010; 51: 3649
    • 5c Das B, Balasubramanyam P, Reddy GC, Salvanna N. Helv. Chim. Acta 2011; 94: 1347
    • 6a Shanthi G, Perumal PT. Tetrahedron Lett. 2007; 48: 6785
    • 6b Chen WL, Cai YF, Fu X, Liu XH, Lin LL, Feng XM. Org. Lett. 2011; 13: 4910
  • 7 Lakshmi NV, Kiruthika SE, Perumal PT. Synlett 2011; 1389
    • 8a Yin GD, Wang ZH, Chen AH, Gao M, Wu AX, Pan YJ. J. Org. Chem. 2008; 73: 3377
    • 8b Yin GD, Liu Q, Ma JR, She NF. Green Chem. 2012; 14: 1796
    • 8c Gao QH, Zhu YP, Lian M, Liu MC, Yuan JJ, Yin GD, Wu AX. J. Org. Chem. 2012; 77: 9865
    • 8d Lian M, Li Q, Zhu YP, Yin GD, Wu AX. Tetrahedron 2012; 68: 9598
    • 8e Yin GD, Fan L, Ren TB, Zheng CY, Tao Q, Wu AX, She NF. Org. Biomol. Chem. 2012; 12: 8877
  • 9 Heffernan GD, Coghlan RD, Manas ES, McDevitt RE, Li Y, Mahaney PE, Robichaud AJ, Huselton C, Alfinito P, Bray JA, Cosmi SA, Johnston GH, Kenney T, Koury E, Winneker RC, Deecher DC, Trybulski EJ. Bioorg. Med. Chem. 2009; 17: 7802
  • 10 Ivachtchenko AV, Golovina ES, Kadieva MG, Koryakova AG, Kovalenko SM, Mitkin OD, Okun IM, Ravnyeyko IM, Tkachenko SE, Zaremba OV. Bioorg. Med. Chem. 2010; 18: 5282
  • 11 Dias TA, Proença MF. Tetrahedron Lett. 2012; 53: 5235
  • 12 Curini M, Epifano F, Chimichi S, Montanari F, Nocchetti M, Rosati O. Tetrahedron Lett. 2005; 46: 3497
  • 13 Elinson MN, Dorofeev AS, Miloserdov FM, Ilovaisky AI, Feducovich SK, Belyakov PA, Nikishin GI. Adv. Synth. Catal. 2008; 350: 591
  • 14 Crystallographic data for compound 5o have been deposited with the accession number CCDC 901984, and can be obtained free of charge from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; Fax: +44(1223)336033; E-mail: deposit@ccdc.cam.ac.uk; Web site: www.ccdc.cam.ac.uk/conts/retrieving.html.
    • 15a Xie JW, Huang X, Fan LP, Xu DC, Li XS, Su H, Wen YH. Adv. Synth. Catal. 2009; 351: 3077
    • 15b Pattan SR, Dighe NS, Musmade DS, Gaware VM, Jadhav SG, Khade MA, Hiremath SN. Asian J. Res. Chem. 2010; 3: 126
  • 16 Li XF, Cun LF, Lian CX, Zhong L, Chen YC, Liao J, Zhu J, Deng JG. Org. Biomol. Chem. 2008; 6: 349
    • 17a Liu YB, Liu XH, Wang M, He P, Lin LL, Feng XM. J. Org. Chem. 2012; 77: 4136
    • 17b Sashidhara KV, Kumar A, Agarwal S, Kumar M, Kumar B, Sridhar B. Adv. Synth. Catal. 2012; 354: 1129
    • 17c Nagarathnam D, Cushman M. Tetrahedron 1991; 47: 5071
    • 17d Verma AK, Pratap R. Tetrahedron 2012; 68: 8523