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Synlett 2015; 26(14): 2009-2013
DOI: 10.1055/s-0034-1381050
DOI: 10.1055/s-0034-1381050
letter
Unexpected Metal-Free Fluorination and Oxidation at the C-4 Position of Pyrazoles Promoted by Selectfluor
Further Information
Publication History
Received: 05 May 2015
Accepted after revision: 25 June 2015
Publication Date:
10 August 2015 (online)
Abstract
Metal-free electrophilic fluorination, promoted by Selectfluor, of pyrazoles with methylene groups (CH2X), in which X = OH, OMe, F, N3, and NHMe at the C-4 position furnished the 4-fluoro-pyrazole products from unexpected C–C bond cleavage, at moderate to good yields. Otherwise, under the same reaction conditions, when X = NEt2 or SPr, the oxidation product 4-formyl-pyrazole was obtained.
Key words
electrophilic fluorination - oxidation - Selectfluor - metal-free - pyrazole - hydrazine - Vilsmeier–HaackSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0034-1381050.
- Supporting Information
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References and Notes
- 1a Surmont R, Verniest G, De Scrijver M, Thuring JW, ten Holte P, Deroose F, De Kimpe N. J. Org. Chem. 2011; 76: 4105
- 1b Skinner PJ, Cherrier MC, Webb PJ, Shin YJ, Gharbaoui T, Lindstrom A, Hong V, Tamura SY, Dang HT, Pride CC, Chen R, Richman JG, Connolly DT, Semple G. Bioorg. Med. Chem. Lett. 2007; 17: 5620
- 1c McGrath NA, Brichacek M, Njardarson JT. J. Chem. Educ. 2010; 87: 1348
- 1d Augner D, Gerbino DC, Slavov N, Neudorfl J.-M, Schmalz HG. Org. Lett. 2011; 13: 5374
- 1e Comins D, Schilling S, Zhang Y. Org. Lett. 2005; 7: 95
- 1f Stuk TL, Assink BK, Bates RC, Erdman DT, Fedij V, Jennings SM, Lassig JA, Smith RJ, Smith TL. Org. Process Res. Dev. 2003; 7: 851
- 1g Belliotti TR, Brink WA, Kesten SR, Rubin JR, Wustrow DJ, Zoski KT, Whetzel SZ, Corbin AE, Pugsley TA, Heffner TG, Wise LD. Bioorg. Med. Chem. Lett. 1998; 8: 1499
- 2a Kirk KL. Org. Process Res. Dev. 2008; 12: 305
- 2b Hagmann WK. J. Med. Chem. 2008; 51: 4359
- 2c Müller K, Faeh C, Diederich F. Science 2007; 317: 1881
- 3 Giornal F, Pazenok S, Rodefeld L, Lui N, Vors J.-P, Leroux FR. J. Fluorine Chem. 2013; 152: 2
- 4a Levy M, Zylber-Katz E, Rosenkranz B. Clin. Pharmacokinet. 1995; 28: 216
- 4b Lorenzetti BB, Ferreira SH. Eur. J. Pharmacol. 1985; 114: 375
- 5a Sloop JC, Jackson JL, Schmidt RD. Heteroat. Chem. 2009; 20: 341
- 5b Surmont R, Verniest G, De Kimpe N. Org. Lett. 2010; 12: 4648
- 6 Breen JR, Sandford G, Yufit DS, Howard JA. K, Fray J, Patel B. Beilstein J. Org. Chem. 2011; 7: 1048
- 7 Qian J, Liu Y, Zhu J, Jiang B, Xu Z. Org. Lett. 2011; 13: 4220
- 8a Martins MA. P, Frizzo CP, Tier AZ, Moreira DN, Zanatta N, Bonacorso HG. Chem. Rev. 2014; 114: PR1
- 8b Bonacorso HG, Paim GR, Porte LM. F, Pittaluga EP, Cavinatto S, Meyer AR, Martins MA. P, Zanatta N. J. Heterocycl. Chem. 2014; 51: 1171
- 8c Bonacorso HG, Navarini J, Porte LM. F, Pittaluga EP, Junges AF, Meyer AR, Martins MA. P, Zanatta N. J. Fluorine Chem. 2013; 151: 38
- 8d Flore AF. C, Brondani S, Pizzuti L, Martins MA. P, Zanatta N, Bonacorso HG. Synthesis 2005; 2744
- 9a Bonacorso HG, Porte LM. F, Navarini J, Paim GR, Luz FM, Oliveira LM, Wiethan CW, Martins MA. P. Zanatta N. Tetrahedron Lett. 2011; 52: 3333
- 9b Bonacorso HG, Porte LM. F, Paim GR, Luz FM, Martins MA. P. Zanatta N. Tetrahedron Lett. 2010; 51: 3759
- 9c Bonacorso HG, Porte LM. F, Cechinel CA, Paim GR, Deon ED, Zanatta N, Martins MA. P. Tetrahedron Lett. 2009; 50: 1392
- 10a Cotesta S, Furet P, Guagnano V, Holzer P, Kallen J, Mah R, Masuya K, Schlapbach A, Stutz S, Vaupel A. WO 2013175417 A1, 2013
- 10b Takaoka A, Ibrahim MK, Kagaruki SR. F, Ishikawa N. Nipon Kagaku Kaishi 1985; 11: 2169
- 10c Kagaruki SR. F, Kitazume T, Ishikawa NB. Chem. Soc. Jpn. 1981; 54: 3221
- 11 Dinoiu V. Rev. Roum. Chim. 2007; 52: 219
- 12 Takeuchi Y, Tarui T, Shibata N. Org. Lett. 2000; 2: 639
- 13a Kira MA, Abdel-Rahman MO, Gadalla KZ. Tetrahedron Lett. 1969; 10: 109
- 13b Rathelot P, Azas N, El-Kashef H, Delmas F, Giorgio C, Timon-David P, Maldonado J, Vanelle P. Eur. J. Med. Chem. 2002; 37: 671
- 14 Ye C, Shreeve JM. J. Org. Chem. 2004; 69: 8561
- 15 Cong Z.-Q, Wang C.-I, Chen T, Yin B.-Z. Synth. Commun. 2006; 36: 679
- 16a Bratenko MK, Chornous VA, Vovk MV. Russ. J. Org. Chem. 2002; 38: 411
- 16b Bonacorso HG, Navarini J, Luz FM, Wiethan CW, Junges AF, Cavinatto S, Martins MA. P, Zanatta N. J. Fluorine Chem. 2013; 146: 53
- 17 General Procedure with Selectfluor (4b, 8) Selectfluor (1.1 mmol) was added to a pyrazole solution (10–12, 15–18, 1 mmol) in anhydrous MeCN (5 mL). After the addition, the reaction mixture was stirred at reflux for 2 h and cooled to r.t. Distilled H2O (15 mL) was then added under magnetic stirring and extracted with CHCl3 (2 × 15 mL). The organic layer was washed with distilled H2O (2 × 20 mL) and brine (1 × 20 mL), dried over Na2SO4, and the solvent was evaporated under reduced pressure. Products 8a–c were purified by silica gel column chromatography, using a mixture of hexane–EtOAc (95:5 v/v) as eluent.
- 18 4-Fluoro-3-(4-nitrophenyl)-1H-1-phenylpyrazole (8b) Yellow solid; yield 65%; mp 135–137 °C. 1H NMR (400.13 MHz, CDCl3): δ = 8.28 (d, J = 9.0 Hz, 2 H), 8.10 (d, J = 8.8 Hz, 2 H), 7.90 (d, 2 J = 4.4 Hz, 1 H), 7.69 (d, J = 7.8 Hz, 2 H), 7.48 (t, J = 8.3 Hz, 2 H), 7.34 (t, J = 7.3 Hz, 1 H). 19F NMR (376.3 MHz, CDCl3): δ = –169.9 (d, J = 4.2 Hz). 13C NMR (100.61 MHz, CDCl3): δ = 150.6 (d, J = 254 Hz), 147.2, 139.6, 137.0 (d, 3 J = 3.8 Hz), 136.6 (d, 2 J = 6.1 Hz), 129.6, 127.2, 126.5 (d, 4 J = 4.4 Hz), 124.0, 118.7, 114.7 (d, 2 J = 30 Hz). Anal. Calcd for C15H10FN3O2 (283.07): C, 63.60; H, 3.56; N, 14.83. Found: C, 63.60; H, 3.29; N, 14.83.
- 19 Rajawinslin RR, Raihan MJ, Janreddy D, Kavala V, Kuo C.-S, Kuo T.-S, Chen M.-L, He C.-H, Yao C.-F. Eur. J. Org. Chem. 2013; 5743
- 20 Bonacorso HG, Navarini J, Porte LM. F, Pittaluga EP, Junges AF, Meyer AR, Martins MA. P, Zanatta N. J. Fluorine Chem. 2013; 151: 38
- 21 Stavber S. Molecules 2011; 16: 6432
- 22 Kirihara M, Naito S, Ishizuka Y, Hanai H, Noguchi T. Tetrahedron Lett. 2011; 52: 3086
- 23 Jin Z, Xu B, Hammond GB. Tetrahedron Lett. 2011; 52: 1956
- 24 Stavber S, Zupan M. Acta Chim. Slov. 2005; 52: 13
- 25a Serguchev YA, Ponomarenko MV, Lourie LF, Fokin AA. J. Phys. Org. Chem. 2011; 24: 407
- 25b Yang Q, Mao L.-L, Yang B, Yang S.-D. Org. Lett. 2014; 16: 3460
- 25c Li Z, Zhang C, Zhu L, Liu C, Li C. Org. Chem. Front. 2014; 1: 100
- 25d Vincent SP, Burkart MD, Tsai C.-Y, Zhang Z, Wong C.-H. J. Org. Chem. 1999; 64: 5264
- 25e Nyffeler PT, Durón SG, Burkart MD, Vincent SP, Wong C.-H. Angew. Chem. Int. Ed. 2005; 44: 192
- 26a Borodkin GI, Zaikin PA, Shubin VG. Tetrahedron Lett. 2006; 47: 2639
- 26b Borodkin GI, Zaikin PA, Shakirov MM, Shubin VG. Russ. J. Org. Chem. 2007; 43: 1451
- 27 Eicher T, Hauptmann S. The Chemistry of Heterocycles – Structure, Reactions, Syntheses and Applications. Wiley-VCH; Weinheim: 2003. 2nd ed.
- 28 Breen JR, Sandford G, Patel B, Fray J. Synlett 2015; 26: 51
- 29a Zupan M, Iskra J, Stavber S. Bull. Chem. Soc. Jpn. 1995; 68: 1655
- 29b Banks RE, Lawrence NJ. Popplewell A. L. Synlett 1994; 831
- 29c Wang H, Ren S, Zhang J, Zhang W, Liu Y. J. Org. Chem. 2015; 80: 6856
- 30 Zhang J, Wang H, Ren S, Zhang W, Liu Y. Org. Lett. 2015; 17: 2920