Synthesis 2016; 48(23): 4260-4268
DOI: 10.1055/s-0035-1562611
paper
© Georg Thieme Verlag Stuttgart · New York

Transition-Metal-Free Terminal Alkyne Addition to Isatins

Kalyan Dhara
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India   eMail: ocjd@iacs.res.in
,
Ajoy Kapat
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India   eMail: ocjd@iacs.res.in
,
Tridev Ghosh
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India   eMail: ocjd@iacs.res.in
,
Jyotirmayee Dash*
Department of Organic Chemistry, Indian Association for the Cultivation of Science, Jadavpur, Kolkata 700032, India   eMail: ocjd@iacs.res.in
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Publikationsverlauf

Received: 20. Mai 2016

Accepted after revision: 11. Juli 2016

Publikationsdatum:
24. August 2016 (online)


Abstract

A ‘direct’ alkynylation of isatins, which uses potassium tert-butoxide to provide the desired 3-hydroxy-3-ethynyl-2-oxindoles in good to high yields, is reported. This protocol proceeds smoothly for both electron-rich and electron-deficient alkynes in comparable reaction rates and does not require any specially design ligand or expensive transition-metal catalysts.

Supporting Information

 
  • References

  • 1 Trost BM. Science 1991; 254: 1471
  • 2 Paladhi S, Bhati M, Panda D, Dash J. J. Org. Chem. 2014; 79: 1473
    • 3a Suzuki H, Morita H, Shiro M, Kobayashi J. Tetrahedron 2004; 60: 2489
    • 3b Kamano Y, Zhang H.-P, Ichihara Y, Kizu H, Komiyama K, Pettit GR. Tetrahedron Lett. 1995; 36: 2783
    • 3c Kawasaki T, Nagaoka M, Satoh T, Okamoto A, Ukon R, Ogawa A. Tetrahedron 2004; 60: 3493
    • 3d Miah S, Moody CJ, Richards IC, Slawin AM. Z. J. Chem. Soc., Perkin Trans. 1 1997; 2405
    • 3e Rasmussen HB, MacLeod JK. J. Nat. Prod. 1997; 60: 1152
  • 4 Boechat N, Kover WB, Bongertz V, Bastos MM, Romeiro NC, Azevedo ML. G, Wollinger W. Med. Chem. (Sharjah, United Arab Emirates) 2007; 3: 533

    • For alkyne addition to carbonyls, see:
    • 5a Trost BM, Weiss AH. Adv. Synth. Catal. 2009; 351: 963
    • 5b Carreira EM, Frantz DE In Science of Synthesis: Stereoselective Synthesis . Vol. 2. Molander GA. Thieme; Stuttgart: 2011: 497
    • 5c Li C.-J. Acc. Chem. Res. 2010; 43: 581

      For alkyne addition to ketones, see:
    • 6a Tzalis D, Knochel P. Angew. Chem. Int. Ed. 1999; 38: 1463
    • 6b Chen C.-Y, Tiller RD, Grabowski EJ. J, Reider PJ. Angew. Chem. Int. Ed. 1999; 38: 711
    • 6c Choudhury A, Moore JR, Pierce ME, Fortunak JM, Valvis I, Confalone PN. Org. Process Res. Dev. 2003; 7: 324
    • 6d Jiang B, Tang X. Org. Lett. 2002; 4: 3451
    • 6e Dhondi PK, Chisholm JD. Org. Lett. 2006; 8: 67
    • 6f Dhondi PK, Carberry P, Choi LB, Chisholm JD. J. Org. Chem. 2007; 72: 9590
    • 6g Motoki R, Kanai M, Shibasaki M. Org. Lett. 2007; 9: 2997
    • 6h Deng G.-J, Li C.-J. Synlett 2008; 1571
    • 6i Brummond KM, Osbourn JM. Beilstein J. Org. Chem. 2010; 6: 33
    • 6j Chinkov N, Warm A, Carreira EM. Angew. Chem. Int. Ed. 2011; 50: 2957

      For catalytic alkyne addition to ketones, see:
    • 7a Cozzi PG. Angew. Chem. Int. Ed. 2003; 42: 2895
    • 7b Lu G, Li X, Jia X, Chan WL, Chan AS. C. Angew. Chem. Int. Ed. 2003; 42: 5057
    • 7c Saito B, Katsuki T. Synlett 2004; 1557
    • 7d Cozzi PG, Alesi S. Chem. Commun. 2004; 2448
    • 7e Liu L, Wang R, Kang Y.-F, Chen C, Xu Z.-Q, Zhou Y.-F, Ni M, Cai H.-Q, Gong M.-Z. J. Org. Chem. 2005; 70: 1084

      Reference for alkyne addition to aldehydes, see:
    • 8a Viehe HG, Reinstein M. Chem. Ber. 1962; 95: 2557
    • 8b Brandsma L. Preparative Acetylenic Chemistry. 2nd ed. Elsevier; Amsterdam: 1988
    • 8c Wang Q, Pu L. Synlett 2013; 24: 1340
  • 9 Chen G, Wang Y, Guo S, He H.-P, Li S.-L, Zhang J.-X, Ding J, Hao X.-J. J. Heterocycl. Chem. 2009; 46: 217
  • 10 Fu X.-P, Liu L, Wang D, Chen Y.-J, Li C.-J. Green Chem. 2011; 13: 549
  • 11 Chouhan M, Senwar KR, Kumar K, Sharma R, Nair VA. Synthesis 2014; 46: 195
  • 12 Midya GC, Kapat A, Maiti S, Dash J. J. Org. Chem. 2015; 80: 4148
  • 13 Babler JH, Liptak VP, Phan N. J. Org. Chem. 1996; 61: 416
    • 14a Burke MD, Schreiber SL. Angew. Chem. Int. Ed. 2004; 43: 46
    • 14b O’Connor CJ, Beckmann HS. G, Spring DR. Chem. Soc. Rev. 2012; 41: 4444
  • 15 Bew SP, Hiatt-Gipson GD, Lovell JA, Poullain C. Org. Lett. 2012; 14: 456

    • A stoichiometric amount of 18-crown-6 was added to the alkynylation reaction of isatin 1a with phenylacetylene (2a) under the standard reaction conditions. The reaction afforded 3aa in 60% yield, a 20% inhibition of product formation compared to the reaction in the absence of 18-crown-6 (Table 1, entry 7). Only partial inhibition of the product yield was observed; possibly toluene is not the best solvent for efficient 1:1 complex formation; see:
    • 16a Izzat RM, Pawlak K, Bradshaw JS. Chem. Rev. 1991; 91: 1721
    • 16b Li Y, Huszthy P, Móczár I, Szemenyei B, Kunsági-Máté S. Chem. Phys. Lett. 2013; 556: 94
  • 17 Different aryl ketones (benzaldehydes, acetophenone, trifluoroacetophenone) and aryl diketones (benzil and 9,10-phenanthrenequinone) were used as the electrophilic partner. As expected, none of these substrates, except trifluoroacetophenone, afforded the corresponding addition products. The aryl ketone trifluoroacetophenone, due to its high electrophilicity, provided the desired product in low (30%) yield. Under similar reaction conditions, the alkynylation of acetone with phenyl­acetylene did not proceed to give the desired product.
  • 18 CCDC 1433098 contains the supplementary crystallographic data for 3da in this paper. The data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/getstructures.