Synthesis 2020; 52(09): 1398-1406
DOI: 10.1055/s-0039-1690053
paper
© Georg Thieme Verlag Stuttgart · New York

Synthesis of 4-Nitroisoxazoles via NO/NO2-Mediated Heterocyclization of Aryl-Substituted α,β-Unsaturated Ketones

Dmitry A. Vasilenko
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Kirill S. Sadovnikov
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Kseniya N. Sedenkova
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
b   Institute of Physiologically Active Compounds, Severny Proezd 1, Chernogolovka, Moscow Region 142432, Russian Federation
,
Anastasiya V. Kurova
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Yuri K. Grishin
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Tamara S. Kuznetsova
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Victor B. Rybakov
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
,
Yulia A. Volkova
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
c   N.D. Zelinsky Institute of Organic Chemistry RAS, Leninsky Prospect, 47, Moscow 119991, Russian Federation
,
Elena B. Averina
a   Department of Chemistry, Lomonosov Moscow State University, Leninskie Gory 1 bd. 3, Moscow 119991, Russian Federation   Email: elaver@med.chem.msu.ru
b   Institute of Physiologically Active Compounds, Severny Proezd 1, Chernogolovka, Moscow Region 142432, Russian Federation
› Author Affiliations
This work was supported by the Russian Science Foundation, grant no. 19-73-00145.
Further Information

Publication History

Received: 10 December 2019

Accepted after revision: 13 January 2020

Publication Date:
03 February 2020 (online)


Abstract

A straightforward approach for the synthesis of 4-nitroisoxazoles has been developed via heterocyclization of aryl/hetaryl-substituted α,β-unsaturated ketones upon treatment with tetranitromethane-triethylamine (TNM-TEA) complex or t-BuONO. This strategy features high efficiency and wide substrate tolerance under simple reaction conditions.

Supporting Information

Primary Data

 
  • References


    • For reviews and some recent examples, see:
    • 1a Cordero FM, Giomi D, Lascialfari L. In Progress in Heterocyclic Chemistry, Vol. 27. Gribble G, Joule J. Elsevier; Amsterdam: 2015: 321
    • 1b Hamama WS, Ibrahim ME, Zoorob HH. Synth. Commun. 2013; 43: 2393
    • 1c Fuse S, Morita T, Nakamura H. Synthesis 2017; 49: 2351
    • 1d Morita T, Yugandar S, Fuse S, Nakamura H. Tetrahedron Lett. 2018; 59: 1159
    • 1e Hu F, Szostaka M. Adv. Synth. Catal. 2015; 357: 2583
    • 1f Galenko AV, Khlebnikov AF, Novikov MS, Pakalnis VV, Rostovskii NV. Russ. Chem. Rev. 2015; 84; 335; Usp. Khim. 2015, 84, 335
    • 1g Dighe SU, Mukhopadhyay S, Kolle S, Kanojiya S, Batra S. Angew. Chem. Int. Ed. 2015; 54: 10926
    • 1h Fu M, Li H, Su M, Cao Z, Liu Y, Liu Q, Guo C. Adv. Synth. Catal. 2019; 361: 3420
    • 2a Barmade MA, Murumkar PR, Sharma MK, Yadav MR. Curr. Top. Med. Chem. 2016; 16: 2863
    • 2b Uto Y. Curr. Pharm. Des. 2016; 22: 3201
    • 2c Sysak A, Obmińska-Mrukowicz B. Eur. J. Med. Chem. 2017; 137: 292
    • 2d Zhu J, Mo J, Lin HZ, Chen Y, Sun HP. Bioorg. Med. Chem. 2018; 23: 3065
    • 3a Doi Y, Chambers HF. In Mandell, Douglas, and Bennett's Principles and Practice of Infectious Diseases, 8th ed., Vol. 1. Bennett JE, Dolin R, Blaser MJ. Elsevier Saunders; Philadelphia: 2015: 263
    • 3b Farrington M. In Clinical Pharmacology, 11th ed. Bennett PN, Brown MJ, Sharma P. Elsevier Ltd; Churchill Livingstone: 2012: 173
  • 4 Leppik IE. Seizure 2004; 13S1: S5
  • 5 Leucht S, Cipriani A, Spineli L, Mavridis D, Örey D, Richter F, Samara M, Barbui C, Engel RR, Geddes JR, Kissling W, Stapf MP, Lässig B, Salanti G, Davis JM. Lancet 2013; 382: 951
  • 6 Larsen JK, Rafaelsen OJ. Acta Psych. Scand. 1980; 62: 456
  • 7 Liu Y.-Y, Hsiao H.-T, Wang JC.-F, Liu Y.-C, Wu S.-N. Eur. J. Pharm. 2019; 844: 95
  • 8 Sanders S, Harisdangkul V. Am. J. Med. Sci. 2002; 323: 190
    • 9a Zimecki M, Bąchor U, Mączyński M. Molecules 2018; 23: 2724
    • 9b Averina EB, Vasilenko DA, Gracheva YA, Grishin YK, Radchenko EV, Burmistrov VV, Butov GM, Neganova ME, Serkova TP, Redkozubova OM, Shevtsova EF, Milaeva ER, Kuznetsova TS, Zefirov NS. Bioorg. Med. Chem. 2016; 24: 712
  • 10 Jensen AA, Plath N, Pedersen MH. F, Isberg V, Krall J, Wellendorph P, Stensbol TB, Gloriam DE, Krogsgaard-Larsen P, Frølund B. J. Med. Chem. 2013; 56: 1211
    • 11a Drysdale MJ, Dymock BW, Finch H, Webb P, Mcdonald E, James KE, Cheung KM, Mathews TP. WO2004072051 A1, 2004 ; Chem. Abstr. 2004, 141, 696360
    • 11b Vasilenko DA, Averina EB, Zefirov NA, Wobith B, Grishin YK, Rybakov VB, Zefirova ON, Kuznetsova TS, Kuznetsov SA, Zefirov NS. Mendeleev Commun. 2017; 27: 228
  • 12 Vasilenko DA, Dueva EV, Kozlovskaya LI, Zefirov NA, Grishin YK, Butov GM, Palyulin VA, Kuznetsova TS, Karganova GG, Zefirova ON, Osolodkin DI, Averina EB. Bioorg. Chem. 2019; 87: 629
  • 13 Madsen U, Bang-Andersen B, Brehm L, Christensen IT, Ebert B, Kristoffersen IT. S, Lang Y, Krogsgaard-Larsen P. J. Med. Chem. 1996; 39: 1682
  • 14 Jorgensen AT, Tagmose L, Stensbol TB, Vestergaard HT, Engblom C, Kristiansen U, Sanchez C, Krogsgaard-Larsen P, Liljefors T. J. Med. Chem. 2002; 45: 2454
  • 15 Simoni D, Rondanin R, Baruchello R, Rizzi M, Grisolia G, Eleopra M, Grimaudo S, Di Cristina A, Pipitone MR, Bon-giorno MR, Arico M, Invidiata FP, Tolomeo M. J. Med. Chem. 2008; 51: 4796
  • 16 Srinivas A, Nagaraj A, Reddy CS. J. Heterocycl. Chem. 2009; 46: 497
    • 17a The Nitro Group in Organic Synthesis . Ono N. Wiley-VCH; New York: 2001: 372
    • 17b Denmark SE, Cottell JJ. In The Chemistry of Heterocyclic Compounds, Synthetic Applications of 1,3-Dipolar Cycloaddition Chemistry Toward Heterocycles and Natural Products, Vol. 59. Padwa A, Pearson WH. Wiley; New York: 2002: 83
    • 17c Ioffe SL. In Nitrile Oxide, Nitrones and Nitronates in Organic Synthesis, 2nd ed. Feuer H. Wiley-VCH; Weinheim: 2008: 435
    • 17d Halimehjani AZ, Namboothiri IN. N, Hooshmand SE. RSC Adv. 2014; 4: 48022
    • 18a Zhang Y, Wei B, Lin H, Cui W, Zeng X, Fan X. Adv. Synth. Catal. 2015; 357: 1299
    • 18b Xia X, Zhu Q, Wang J, Chen J, Cao W, Zhu B, Wu X. J. Org. Chem. 2018; 83: 14617
    • 18c Zhu B, Lee R, Yin Y, Li F, Coote ML, Jiang Z. Org. Lett. 2018; 20: 429
    • 18d Zhu B, Li F, Lu B, Chang J, Jiang Z. J. Org. Chem. 2018; 83: 11350
  • 19 Adamo MF. A, Nagabelli M. Org. Lett. 2008; 10: 1807
  • 20 Rajanarendar E, Reddy MN, Reddy KG, Krishna SR. Tetrahedron Lett. 2012; 53: 2909
    • 21a Reddy MS, Chowhan LR, Kumar NS, Ramesh P, Mukkamala SB. Tetrahedron Lett. 2018; 59: 1366
    • 21b Reddy MS, Kumar NS, Chowhan LR. RSC Adv. 2018; 8: 35587
    • 21c Liu K, Xiong Y, Wang Z.-F, Tao H.-Y, Wang C.-J. Chem. Commun. 2016; 52: 9458
    • 22a Nagaraju S, Satyanarayana N, Paplal B, Vasu AK, Kanvah S, Sridhar B, Sripadi P, Kashinath D. RSC Adv. 2015; 5: 94474
    • 22b Zhang J, Liu X, Ma X, Wang R. Chem. Commun. 2013; 49: 9329
    • 22c Baschieri A, Bernardi L, Ricci A, Suresh S, Adamo MF. A. Angew. Chem. Int. Ed. 2009; 48: 9342
    • 22d Disetti P, Moccia M, Illera DS, Suresha S, Adamo MF. A. Org. Biomol. Chem. 2015; 13: 10609
    • 22e Rout S, Joshi H, Singh VK. Org. Lett. 2018; 20: 2199
    • 22f Pei Q.-L, Sun H.-W, Wu Z.-J, Du X.-L, Zhang X.-M, Yuan W.-C. J. Org. Chem. 2011; 76: 7849
    • 23a Chen X.-Y, Liu Q, Chauhan P, Li S, Peuronen A, Rissanen K, Jafari E, Enders D. Angew. Chem. Int. Ed. 2017; 56: 6241
    • 23b Chen X.-Y, Li S, Sheng H, Liu Q, Jafari E, Essen C, Rissanen K, Enders D. Chem. Eur. J. 2017; 23: 13042
    • 23c Liu X.-L, Han W.-Y, Zhang X.-M, Yuan W.-C. Org. Lett. 2013; 15: 1246
    • 23d Chauhan P, Mahajan S, Raabe G, Enders D. Chem. Commun. 2015; 51: 2270
    • 23e Liu X.-L, Wei Q.-D, Zuo X, Xu S.-W, Yao Z, Wang J.-X, Zhou Y. Adv. Synth. Catal. 2019; 361: 2836
    • 23f Suresh A, Baiju TV, Kumar T, Namboothiri IN. N. J. Org. Chem. 2019; 84: 3158
  • 24 Vasilenko DA, Sedenkova KN, Kuznetsova TS, Averina EB. Synthesis 2019; 51: 1516
    • 25a Volkova YA, Averina EB, Grishin YK, Bruheim P, Kuznetsova TS, Zefirov NS. J. Org. Chem. 2010; 75: 3047
    • 25b Averina EB, Volkova YA, Samoilichenko YV, Grishin YK, Rybakov VB, Kutateladze AG, Elyashberg ME, Kuznetsova TS, Zefirov NS. Tetrahedron Lett. 2012; 53: 1472
    • 25c Averina EB, Vasilenko DA, Samoilichenko YV, Grishin YK, Rybakov VB, Kuznetsova TS, Zefirov NS. Synthesis 2014; 46: 1107
    • 25d Volkova YA, Averina EB, Vasilenko DA, Sedenkova KN, Grishin YuK, Bruheim P, Kuznetsova TS, Zefirov NS. J. Org. Chem. 2019; 84: 3192

      For recent examples of various bioactive bis(heterocycles), see:
    • 26a Drapier T, Geubelle P, Bouckaert C, Nielsen L, Laulumaa S, Goffin E, Dilly S, Francotte P, Hanson J, Pochet L, Kastrup JS, Pirotte B. J. Med. Chem. 2018; 61: 5279
    • 26b Venkatraj M, Salado IG, Heeres J, Joossens J, Lewi PJ, Caljon G, Maes L, Veken P, Augustyns K. Eur. J. Med. Chem. 2018; 143: 306
    • 26c Dai H, Ge S, Guo J, Chen S, Huang M, Yang J, Sun S, Ling Y, Shi Y. Eur. J. Med. Chem. 2018; 143: 1066
    • 27a Altukhov KV, Perekalin VV. Usp. Khim. 1976; 45: 2050 ; Chem. Abstr. 1977, 86, 71774s
    • 27b Nielsen AT. Nitrocarbons. Wiley-VCH; Weinheim: 1995: 190
    • 27c Nazin GM, Manelis GB. Russ. Chem. Rev. 1994; 63: 313
  • 28 Khisamutdinov GK, Lyapin NM, Nikitin VG, Slovetskii VI, Fainzil’berg AA. Russ. Chem. Bull. 2009; 58: 2178

    • For review and recent examples, see:
    • 29a Li P, Jia X. Synthesis 2018; 50: 711
    • 29b He Y, Feng T, Fan X. Org. Lett. 2019; 21: 3918
    • 29c Dai P, Tan X, Luo Q, Yu X, Zhang S, Liu F, Zhang W.-H. Org. Lett. 2019; 21: 5096
    • 29d Sau P, Rakshit A, Alam T, Srivastava KH, Patel BK. Org. Lett. 2019; 21: 4966
  • 30 Hauff J.-P, Tuaillon J, Perrot R. Helv. Chim. Acta 1978; 61: 1207
  • 31 Li L, Zhao M.-N, Ren Z.-H, Li J.-L, Guan Z.-H. Org. Lett. 2012; 14: 3506
  • 32 Cheng Y.-F, Dong X.-Y, Gu Q.-S, Yu Z.-L, Liu X.-Y. Angew. Chem. Int. Ed. 2017; 56: 8883
  • 33 Kesten SJ, Degnan MJ, Hung J, McNamara DJ, Ortwine DF, Uhlendorf SE, Werbel LM. J. Med. Chem. 1992; 35: 3429
  • 34 Canela M.-D, Pérez-Pérez M.-J, Noppen S, Sáez-Calvo G, Díaz JF, Camarasa M.-J, Liekens S, Priego E.-M. J. Med. Chem. 2014; 57: 3924
  • 35 Adeva M, Sahagún H, Caballero E, Clairac RP.-L, Medarde M, Tomé F. J. Org. Chem. 2000; 65: 3387
  • 36 Louie T, Goodman D, Holloway GA, McFadden GI, Mollard V, Watson KG. Bioorg. Med. Chem. Lett. 2010; 20: 4611
  • 37 Shih J.-L, Nguyen TS, May JA. Angew. Chem. Int. Ed. 2015; 54: 9931
  • 38 Zhang S.-L, Denga Z.-Q. Org. Biomol. Chem. 2016; 14: 7282
  • 39 Pesciaioli F, Vincentiis F, Galzerano P, Bencivenni G, Bartoli G, Mazzanti A, Melchiorre P. Angew. Chem. Int. Ed. 2008; 47: 8703
  • 40 Wei H, Li Y, Xiao K, Cheng B, Wang H, Hu L, Zhai H. Org. Lett. 2015; 17: 5974
  • 41 Le PQ, Nguyen TS, May JA. Org. Lett. 2012; 14: 6104
  • 42 Sawada M, Kubo S, Matsumura K, Takemoto Y, Kobayashi H, Tashiro E, Kitahara T, Watanabe H, Imoto M. Bioorg. Med. Chem. Lett. 2011; 21: 1385
  • 43 Chang M.-Y, Chen Y.-C, Chan C.-K. Tetrahedron 2014; 70: 2257
  • 44 Kellogg RM, Nieuwenhuijzen JW, Pouwer K, Vries TR, Broxterman QB, Grimbergen RF. P, Kaptein B, Crois RM. L, de Wever E, Zwaagstra K, van der Laan AC. Synthesis 2003; 1626
  • 45 Lawrence NJ, Armitage ES. M, Greedy B, Cook D, Ducki S, McGown AT. Tetrahedron Lett. 2006; 47: 1637
  • 46 Applequist DE, Gdanski RD. J. Org. Chem. 1981; 46: 2502
  • 47 Duranti E, Balsamini C, Spadoni G, Staccioli L. J. Org. Chem. 1988; 53: 2870
  • 48 Quilico A, Fusco R, Rosnati V. Gazz. Chim. Ital. 1946; 76: 30 ; Chem. Abstr. 1947, 41, 2157