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A thermally-induced, tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition approach to carbocyclic spirooxindoles

  1. and
Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, U.S.A
  1. Corresponding author email
Associate Editor: J. Aubé
Beilstein J. Org. Chem. 2010, 6, No. 33. https://doi.org/10.3762/bjoc.6.33
Received 19 Feb 2010, Accepted 31 Mar 2010, Published 08 Apr 2010
Preliminary Communication
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Abstract

The synthesis of C3-carbocyclic spirooxindoles was realized by way of an intramolecular [2 + 2] cycloaddition reaction between a vinylidene indolin-2-one and an alkyne. The cycloaddition reaction occurs selectively with the distal double bond of the allene, is tolerant of a phenyl and trimethylsilyl group on the terminus of the alkyne, and can be used to access bicyclo[4.2.0]octadienes and bicyclo[5.2.0]nonadienes. The allene precursors are not observed, but are likely intermediates of an infrequently encountered thermal [3,3]-sigmatropic rearrangement of a propargylic acetate.

Keywords: allene; propargylic acetate; spirooxindole; thermal [2 + 2] cycloaddition; thermal [3,3]-sigmatropic rearrangement; vinylidene indolin-2-one

Introduction

Spirooxindoles are structural motifs containing a heterocycle or carbocycle at the C3 position of an oxindole. Particularly well known are the pyrrolidinyl-spirooxindoles 1 which have been classified as a privileged motif due to their presence in a large number of heterocyclic alkaloids (Figure 1) [1]. Spirotryprostatin B (2) is just one example of many natural products from this class exhibiting interesting biological activity [2]. Compounds possessing a carbocycle at the C3 position of the oxindole, such as 3, are less common and spirooxindoles containing a four carbon spirocycle are rare. One notable natural product containing this basic skeleton is welwitindolinone A isonitrile (4); a compound that has recently captured the attention of the synthetic community [3,4].

[1860-5397-6-33-1]

Figure 1: Heterocyclic and carbocyclic spirooxindoles.

Spiro[cyclobutane-1,3'-indolin]-2'-ones (3, n = 0) have previously been prepared but the synthetic approach is mostly limited to simple spirocyclobutanes that are accessed via alkylation chemistry [5]. Alternatively, more structurally complex spirocyclobutanes have been obtained from homodimerization reactions of allenes or alkenes [6,7]. However, neither of these approaches provides an enabling strategy for accessing the densely functionalized and unsymmetrical molecular architectures of many of the natural products possessing this oxindoline core. We anticipated that access to this class of compounds utilizing chemistry developed in our laboratories would provide an expansion of substructures within this chemical space, thus enhancing the discovery of new biological probes and pharmaceuticals [8].

We recently disclosed a thermal [2 + 2] cycloaddition reaction of allene-ynes to provide a variety of alkylidene cyclobutenes in good yields [9-18]. Notable features of this reaction were the stability of the resulting alkylidene cyclobutenes, the regioselectivity for reaction of the distal double bond of the allene, and ready cyclization of substrates possessing heteroatom tethers to give heterocyclic structures (Scheme 1) [19-26]. Inspired by the unique skeleton of welwitindolinone A, the feasibility of this method for the preparation of spirooxindole alkaloids was investigated. The preliminary results of this study are reported herein.

[1860-5397-6-33-i1]

Scheme 1: A thermal [2 + 2] cycloaddition reaction.

Results and Discussion

To begin the investigation, the first challenge was the preparation of a functionalized vinylidene indolin-2-one 5 (Figure 2). There is only one report of this allene substructure in the literature and it was not particularly well suited for the incorporation of additional functionality [6]. Scattered reports of propargylic acetates thermally rearranging to allenyl acetates exist, thus, it was reasoned that the allene moiety of 5 could be obtained by way of a thermal [3,3]-sigmatropic rearrangement of the propargylic acetate 6 to give compound 5 where R2 = OAc (Figure 2) [27].

[1860-5397-6-33-2]

Figure 2: Access to vinylidene indolin-2-ones.

Preparation of propargylic acetate 9a was accomplished by the addition of the lithium acetylide of 8 to N-methyl isatin (7) followed by acetylation of the resulting propargyl alcohol. Heating propargylic acetate 9a to 225 °C in 1,2-dichlorobenzene in the microwave for 30 min gave the spirooxindole 10a in 60% yield (Scheme 2). Structural confirmation of 10a was achieved using COSY, HMQC and HMBC. Attempts to effect the [3,3]-sigmatropic rearrangement of the propargyl acetate 9a using transition metal catalysis (AuCl3 10 mol %, toluene, 1 h, rt) led to hydrolysis of the allenyl acetate functionality.

[1860-5397-6-33-i2]

Scheme 2: A tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition.

This densely functionalized alkylidene cyclobutene 10a is postulated to arise via the [2 + 2] cycloaddition reaction between the alkyne and the allenyl acetate in intermediate 11 which in turn arises from the thermal [3,3]-sigmatropic rearrangement of 9a (Figure 3).

[1860-5397-6-33-3]

Figure 3: A tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition.

We have briefly investigated the scope and limitations of this tandem cycloaddition reaction by varying the protecting group on the oxindole nitrogen, altering the substitution on the alkyne terminus and increasing the number of carbon atoms in the tether. Groups such as methyl (Me), methoxymethyl (MOM), and 2-(trimethylsilyl)ethoxymethyl (SEM) were found to be well tolerated. Substrates possessing either a phenyl or a silyl group on the alkyne terminus also gave good yields of the spirooxindoles. However, when a terminal alkyne was subjected to the reaction conditions, only decomposition of the starting material was observed (entry 3, Table 1). When N-methylpyrrolidinone (NMP) was used as a solvent the reaction mixture could be heated to higher temperatures (250 °C vs. 225 °C in 1,2-dichlorobenzene) and the reaction times were shorter which had a marginal affect on the yield of the reaction (compare entries 5 and 6). A further advantage of NMP over 1,2-dichorobenzene was the ease of isolation of the products since the solvent could be removed with aqueous washings instead of column chromatography. To investigate the yield of this reaction the transformation of propargyl acetate 9f to spirooxindole 10f was monitored by proton NMR. We found that the NMR yield is consistent with the isolated yield and the source of lost mass is attributed to decomposition during the course of the reaction as evidenced by baseline impurities on the TLC. However, the only discernable product in the NMR spectrum is the desired spirooxindole 10f.

Table 1: Synthesis of spirooxindoles.

[Graphic 1]
Entry R1 R2 n Solventa Temp Time Product Yield
1 Me Ph 1 1,2-dichlorobenzene 225 °C 30 min 10a 60%
2 Me TMS 1 1,2-dichlorobenzene 225 °C 50 min 10b 50%
3 Me H 1 1,2-dichlorobenzene 225 °C 50 min 10c 0%
4 SEM Ph 1 1,2-dichlorobenzene 225 °C 60 min 10d 61%
5 MOM Ph 1 1,2-dichlorobenzene 225 °C 60 min 10e 57%
6 MOM Ph 1 N-methylpyrrolidinone 250 °C 10 min 10e 61%
7 MOM Ph 2 N-methylpyrrolidinone 250 °C 5 min 10f 48%

aIn our original report, the most successful solvent system for the cycloaddition was toluene doped with an ionic liquid (0.3 M). However we have moved away from this solvent system because subsequent to that study, two sample solutions (out of hundreds), that were allowed to age for an hour prior to microwave irradiation, immediately exploded upon irradiation. Oliver Kappe has made similar observations when using ionic liquids in the presence of ethylene gas in the microwave. Kappe demonstrated that the explosion is due to the ionic liquid initiating an exothermic polymerization reaction [28]. We suspect that the ionic liquid initiated a polymerization reaction of the allene-ynes when allowed to stand prior to irradiation.

Conclusion

We have developed a concise synthesis to C3-carbocyclic spirooxindoles. One important feature of this thermal tandem [3,3]-sigmatropic rearrangement/[2 + 2] cycloaddition reaction is that the reaction remains selective for the distal double bond of the allene even with densely functionalized allenes [29]. In addition, conversion of the propargylic acetate to the spirooxindole in one step provides a rapid and potentially stereoselective increase in molecular complexity. Furthermore, this approach includes a rare example of a thermal [3,3]-sigmatropic rearrangement of a propargylic acetate while metal catalyzed rearrangements of the propargyl acetates are common. Work is currently underway to expand the synthetic utility of this reaction.

Experimental

Spirooxindole (10a) Propargyl acetate 9 (30 mg, 0.081 mmol) was dissolved in 1,2-dichlorobenzene (1.62 mL) in a 0.5–2 mL Biotage™ microwave vial. The vial was capped and the solution irradiated in the microwave for 30 min at 225 °C. The reaction mixture was diluted with hexane (2 mL) and applied to a silica gel column. The column was eluted with hexanes (100 mL) and then with 25% ethyl acetate/hexanes. The fractions containing the desired product were concentrated under reduced pressure to provide 18 mg of spirooxindole 10a as a brown oil in 60% yield.

Supporting Information

General methods, experimental and spectral data are provided for all new compounds in the Supporting Information.

Supporting Information File 1: General methods, experimental and spectral data.
Format: PDF Size: 2.2 MB Download

Acknowledgements

Generous support from the National Science Foundation is gratefully acknowledged (NSF 0910597).

References

  1. Galliford, C. V.; Scheidt, K. A. Angew. Chem., Int. Ed. 2007, 46, 8748. doi:10.1002/anie.200701342
    Return to citation in text: [1]
  2. Cui, C.-B.; Kakeya, H.; Osada, H. Tetrahedron 1996, 52, 12651. doi:10.1016/0040-4020(96)00737-5
    Return to citation in text: [1]
  3. Baran, P. S.; Richter, J. M. J. Am. Chem. Soc. 2005, 127, 15394. doi:10.1021/ja056171r
    Return to citation in text: [1]
  4. Reisman, S. E.; Ready, J. M.; Hasuoka, A.; Smith, C. J.; Wood, J. L. J. Am. Chem. Soc. 2006, 128, 1448. doi:10.1021/ja057640s
    Return to citation in text: [1]
  5. Stevens, F. C.; Bloomquist, W. E.; Borel, A. G.; Cohen, M. L.; Droste, C. A.; Heiman, M. L.; Kriauciunas, A.; Sall, D. J.; Tinsley, F. C.; Jesudason, C. D. Bioorg. Med. Chem. Lett. 2007, 17, 6270. doi:10.1016/j.bmcl.2007.09.011
    Return to citation in text: [1]
  6. Beccalli, E.; Marchesini, A.; Pilati, T. Tetrahedron 1994, 50, 12697. doi:10.1016/S0040-4020(01)89402-3
    Return to citation in text: [1] [2]
  7. Milanesio, M.; Viterbo, D.; Albini, A.; Fasani, E.; Bianchi, R.; Barzaghi, M. J. Org. Chem. 2000, 65, 3416. doi:10.1021/jo991873i
    Return to citation in text: [1]
  8. Lipkus, A. H.; Yuan, Q.; Lucas, K. A.; Funk, S. A.; Bartelt, W. F.; Schenck, R. J.; Trippe, A. J. J. Org. Chem. 2008, 73, 4443. doi:10.1021/jo8001276
    Return to citation in text: [1]
  9. Murakami, M.; Amii, H.; Itami, K.; Ito, Y. Angew. Chem., Int. Ed. Engl. 1995, 34, 1476. doi:10.1002/anie.199514761
    Return to citation in text: [1]
  10. Friesen, R. W.; Dubé, D.; Fortin, R.; Frenette, R.; Prescott, S.; Cromlish, W.; Greig, G. M.; Kargman, S.; Wong, E.; Chan, C. C.; Gordon, R.; Xu, L. J.; Riendeau, D. Bioorg. Med. Chem. Lett. 1996, 6, 2677. doi:10.1016/S0960-894X(96)00501-X
    Return to citation in text: [1]
  11. Lopez, S.; Rodriguez, J.; Rey, J. G.; de Lera, A. R. J. Am. Chem. Soc. 1996, 118, 1881. doi:10.1021/ja9522241
    Return to citation in text: [1]
  12. Delas, C.; Urabe, H.; Sato, F. J. Am. Chem. Soc. 2001, 123, 7937. doi:10.1021/ja016307v
    Return to citation in text: [1]
  13. Paih, J. L.; Dèrien, S.; Bruneau, C.; Demerseman, B.; Toupet, L.; Dixneuf, P. H. Angew. Chem., Int. Ed. 2001, 40, 2912. doi:10.1002/1521-3773(20010803)40:15<2912::AID-ANIE2912>3.0.CO;2-R
    Return to citation in text: [1]
  14. Murakami, M.; Ashida, S.; Matsuda, T. J. Am. Chem. Soc. 2004, 126, 10838. doi:10.1021/ja046429y
    Return to citation in text: [1]
  15. Paih, J. L.; Dérien, S.; Demerseman, B.; Bruneau, C.; Dixneuf, P. H.; Toupet, L.; Dazinger, G.; Kirchner, K. Chem.–Eur. J. 2005, 11, 1312. doi:10.1002/chem.200400899
    Return to citation in text: [1]
  16. Song, Z.; Li, Y.; Liu, M.; Cong, L.; Liu, Y. Organometallics 2006, 25, 5035. doi:10.1021/om060505j
    Return to citation in text: [1]
  17. Ramanathan, S.; Lemal, D. M. J. Org. Chem. 2007, 72, 1570. doi:10.1021/jo061946f
    Return to citation in text: [1]
  18. Yao, L.-F.; Shi, M. Org. Lett. 2007, 9, 5187. doi:10.1021/ol7022592
    Return to citation in text: [1]
  19. Brummond, K. M.; Chen, D. Org. Lett. 2005, 7, 3473. doi:10.1021/ol051115g
    Return to citation in text: [1]
  20. Oh, C. H.; Gupta, A. K.; Park, D. I.; Kim, N. Chem. Commun. 2005, 5670. doi:10.1039/b508306k
    Return to citation in text: [1]
  21. Oh, C. H.; Park, D. I.; Jung, S. H.; Reddy, V. R.; Gupta, A. K.; Kim, Y. M. Synlett 2005, 2092. doi:10.1055/s-2005-871958
    Return to citation in text: [1]
  22. Ohno, H.; Mizutani, T.; Kadoh, Y.; Miyamura, K.; Tanaka, T. Angew. Chem., Int. Ed. 2005, 44, 5113. doi:10.1002/anie.200501413
    Return to citation in text: [1]
  23. Mukai, C.; Hara, Y.; Miyashita, Y.; Inagaki, F. J. Org. Chem. 2007, 72, 4454. doi:10.1021/jo070513p
    Return to citation in text: [1]
  24. Ohno, H.; Mizutani, T.; Kadoh, Y.; Aso, A.; Miyamura, K.; Fujii, N.; Tanaka, T. J. Org. Chem. 2007, 72, 4378. doi:10.1021/jo0700528
    Return to citation in text: [1]
  25. Buisine, O.; Gandon, V.; Fensterbank, L.; Aubert, C.; Malacria, M. Synlett 2008, 751. doi:10.1055/s-2008-1032113
    Return to citation in text: [1]
  26. Ovaska, T. V.; Kyne, R. E. Tetrahedron Lett. 2008, 49, 376. doi:10.1016/j.tetlet.2007.11.042
    Return to citation in text: [1]
  27. Oelberg, D. G.; Schiavelli, M. D. J. Org. Chem. 1977, 42, 1804. doi:10.1021/jo00430a031
    Return to citation in text: [1]
  28. Van der Eycken, E.; Appukkuttan, P.; De Borggraeve, W.; Dehaen, W.; Dallinger, D.; Kappe, C. O. J. Org. Chem. 2002, 67, 7904. doi:10.1021/jo0263216
    Return to citation in text: [1]
  29. Saito, N.; Tanaka, Y.; Sato, Y. Organometallics 2009, 28, 669. doi:10.1021/om801181a
    Return to citation in text: [1]

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