Synthesis
DOI: 10.1055/s-0043-1763690
paper

One-Pot N-α-C(sp3)–H Bond Functionalisation Cascade for the Synthesis of Polysubstituted Imidazoles

Vikas D. Kadu
a   School of Chemical Sciences, Punyashlok Ahilyadevi Holkar Solapur University, Solapur 413255, Maharashtra, India
,
Naga Chandradudu Sankala
b   Department of Chemistry, College of Engineering, Rayalseema University, Kurnool 518002, Andhra Pradesh, India
,
Mahesh G. Hublikar
a   School of Chemical Sciences, Punyashlok Ahilyadevi Holkar Solapur University, Solapur 413255, Maharashtra, India
,
Shahaji I. Bansode
a   School of Chemical Sciences, Punyashlok Ahilyadevi Holkar Solapur University, Solapur 413255, Maharashtra, India
,
Raghunath B. Bhosale
a   School of Chemical Sciences, Punyashlok Ahilyadevi Holkar Solapur University, Solapur 413255, Maharashtra, India
› Author Affiliations


Abstract

A one-pot eco-friendly oxidative N-α-C(sp3)–H bond functionalisation of arylmethylamines for the synthesis of tetrasubstituted imidazoles is demonstrated. The substrate scope of these amines has been well-explored with different substrates, such as 1,2-diketones, an α-hydroxy ketone and phenylacetophenone. In the presence of FeCl3 catalyst and green oxidant O2, the easily accessible substrates afforded tetrasubstituted imidazoles in up to 94% yield.

Supporting Information



Publication History

Received: 29 December 2023

Accepted after revision: 04 March 2024

Article published online:
25 March 2024

© 2024. Thieme. All rights reserved

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References

  • 1 Kabi AK, Sravani S, Gujjarappa R, Garg A, Vodnala N, Tyagi U, Kaldhi D, Velayutham R, Gupta S, Malakar CC. In Nanostructured Biomaterials. Materials Horizons: From Nature to Nanomaterials . Swain BP. Springer; Singapore: 2022: 79
  • 2 Hublikar M, Kadu V, Dublad JK, Raut D, Shirame S, Makam P, Bhosale R. Arch. Pharm. 2020; 353: 2000003
  • 3 Raut DG, Patil SB, Choudhari PB, Kadu VD, Lawand AS, Hublikar MG, Bhosale RB. Curr. Chem. Biol. 2020; 14: 58
  • 4 Raut DG, Patil SB, Kadu VD, Hublikar MG, Bhosale RB. Anti-Cancer Agents Med. Chem. 2018; 18: 2117
  • 5 Raut DG, Bhosale RB, Lawand AS, Hublikar MG, Kadu VD, Patil SB. Recent Adv. Inflammation Allergy Drug Discovery 2022; 16: 19
  • 6 De Luca L. Curr. Med. Chem. 2006; 13: 1
  • 7 Tolomeu HV, Fraga CA. M. Molecules 2023; 28: 838
  • 8 Sharma P, Larosa C, Antwi J, Govindarajan R, Werbovetz KA. Molecules 2021; 26: 4213
  • 9 Zhang L, Peng X.-M, Damu GL. V, Geng R.-X, Zhou C.-H. Med. Res. Rev. 2014; 34: 340
  • 10 Bhowmick NA, Chytil A, Plieth D, Gorska AE, Dumont N, Shappell S, Washington MK, Neilson EG, Moses HL. Science 2004; 303: 848
  • 11 Riduan SN, Zhang Y. Chem. Soc. Rev. 2013; 42: 9055
  • 12 Rani N, Sharma A, Gupta GK, Singh R. Mini-Rev. Med. Chem. 2013; 13: 1626
  • 13 Castelli MV, Butassi E, Monteiro MC, Svetaz LA, Vicente F, Zacchino SA. Expert Opin. Ther. Pat. 2014; 24: 323
  • 14 Gaba M, Mohan C. Med. Chem. Res. 2016; 25: 173
  • 15 Grimmett MR. Adv. Heterocycl. Chem. 1981; 27: 241
  • 16 Sundberg RJ. Chem. Rev. 1974; 74: 471
  • 17 Antolini M, Bozzoli A, Ghiron C, Kennedy G, Rossi T, Ursini A. Bioorg. Med. Chem. Lett. 1999; 9: 1023
  • 18 Gupta P, Hameed S, Jain R. Eur. J. Med. Chem. 2004; 39: 805
  • 19 Uçucu Ü, Karaburun NG, Işikdag I. Farmaco 2001; 56: 285
  • 20 Rocha JA, Andrade IM, Véras LM. C, Quelemes PV, Lima DF, Soares MJ. S, Pinto PL. S, Mayo SJ, Ivanova G, Rangel M, Correia M, Mafud AC, Mascarenhas YP, Delerue-Matos C, de Moraes J, Eaton P, Leite JR. S. A. Phytother. Res. 2017; 31: 624
  • 21 Silva VG, Silva RO, Damasceno SR. B, Carvalho NS, Prudeîncio RS, Aragão KS, Guimarães MA, Campos SA, Véras LM. C, Godejohann M, Leite JR. S. A, Barbosa AL. R, Medeiros JV. R. J. Nat. Prod. 2013; 76: 1071
  • 22 Wang L, Woods KW, Li Q, Barr KJ, McCroskey RW, Hannick SM, Gherke L, Credo RB, Hui Y.-H, Marsh K, Warner R, Lee JY, Zielinski-Mozng N, Frost D, Rosenberg SH, Sham HL. J. Med. Chem. 2002; 45: 1697
  • 23 Evans LE, Cheeseman MD, Yahya N, Jones K. PLoS One 2015; 10: 1
  • 24 Wolkenberg SE, Wisnoski DD, Leister WH, Wang Y, Zhao Z, Lindsley CW. Org. Lett. 2004; 6: 1453
  • 25 Laufer SA, Zimmermann W, Ruff KJ. J. Med. Chem. 2004; 47: 6311
  • 26 Lee JC, Laydon JT, McDonnell PC, Gallagher TF, Kumar S, Green D, McNulty D, Blumenthal MJ, Keys JR, Land vatter SW, Strickler JE, McLaughlin MM, Siemens IR, Fisher SM, Livi GP, White JR, Adams JL, Young PR. Nature 1994; 372: 739
  • 27 Molina P, Tárraga A, Otón F. Org. Biomol. Chem. 2012; 10: 1711
  • 28 Gurjar S, Sharma SK, Sharma A, Ratnani S. Appl. Surf. Sci. Adv. 2021; 6: 100170
  • 29 Cao Y, Zhang R, Cheng T, Guo J, Xian M, Liu H. Appl. Microbiol. Biotechnol. 2017; 101: 521
  • 30 Saheed IO, Azeez SO, Suah FB. M. Carbohydr. Polym. 2022; 298: 120138
  • 31 Meng X, Wang H.-N, Song S.-Y, Zhang H.-J. Chem. Soc. Rev. 2017; 46: 464
  • 32 Ngan VT. T, Chiou P.-Y, Ilhami FB, Bayle EA, Shieh Y.-T, Chuang W.-T, Chen J.-K, Lai J.-Y, Cheng C.-C. Pharmaceutics 2023; 15: 354
  • 33 Zhang F.-M, Dong L.-Z, Qin J.-S, Guan W, Liu J, Li S.-L, Lu M, Lan Y.-Q, Su Z.-M, Zhou H.-C. J. Am. Chem. Soc. 2017; 139: 6183
  • 34 Guo J, Yang Q, Meng Q.-W, Lau CH, Ge Q. ACS Appl. Mater. Interfaces 2021; 13: 6710
  • 35 Li BS, Wen R, Xue S, Shi L, Tang Z, Wang Z, Tang BZ. Mater. Chem. Front. 2017; 1: 646
  • 36 Liu M, Jiang Y, Liu D, Wang J, Ren Z, Russell TP, Liu Y. ACS Energy Lett. 2021; 6: 3228
  • 37 Park S, Kwon O.-H, Kim S, Park S, Choi M.-G, Cha M, Park SY, Jang D.-J. J. Am. Chem. Soc. 2005; 127: 10070
  • 38 Li F.-G, Liu C, Yuan D, Dai F, Wang R, Wang Z, Lu X, Sun D. CCS Chem. 2022; 4: 832
  • 39 Ali R, Dwivedi SK, Mishra H, Misra A. Dyes Pigm. 2020; 175: 108163
  • 40 Zhang Q, Luo L, Xu H, Hu Z, Brommesson C, Wu J, Sun Z, Tian Y, Uvdal K. New J. Chem. 2016; 40: 3456
  • 41 Sahoo A, Deb S, Das S, Baitalik S. Dyes Pigm. 2023; 218: 111425
  • 42 Pavan G, Morgan L, Demitri N, Alberoni C, Scattolin T, Aliprandi A. Chem. Eur. J. 2023; 29: e202301912
  • 43 Felber T, Schaefer T, Herrmann H. J. Phys. Chem. A 2020; 124: 10029
  • 44 Huang H, Ji X, Wu W, Jiang H. Adv. Synth. Catal. 2013; 355: 170
  • 45 Kadu VD, Mali GA, Khadul SP, Kothe GJ. RSC Adv. 2021; 11: 21955
  • 46 Cao J, Zhou X, Ma H, Shi C, Huang G. RSC Adv. 2016; 6: 57232
  • 47 Salfeena CT. F, Jalaja R, Davis R, Suresh E, Somappa SB. ACS Omega 2018; 3: 8074
  • 48 Yang Z, Zhang J, Hu L, Li A, Li L, Liu K, Yang T, Zhou C. J. Org. Chem. 2020; 85: 5952
  • 49 Zhang B, Wan C, Wang Q, Zhang S, Zha Z, Wang Z. Acta Chim. Sin. 2012; 70: 2408
  • 50 Sadeghi B, Mirjalili BB. F, Hashemi MM. Tetrahedron Lett. 2008; 49: 2575
  • 51 Balalaie S, Arabanian A. Green Chem. 2000; 2: 274
  • 52 Heravi MM, Derikvand F, Bamoharram FF. J. Mol. Catal. A: Chem. 2007; 263: 112
  • 53 Chen X, Wang Z, Huang H, Deng GJ. Adv. Synth. Catal. 2018; 360: 4017
  • 54 Donohoe TJ, Kabeshov MA, Rathi AH, Smith IE. D. Org. Biomol. Chem. 2012; 10: 1093
  • 55 Sarkar R, Mukhopadhyay C. Eur. J. Org. Chem. 2015; 1246
  • 56 Claiborne CF, Liverton NJ, Nguyen KT. Tetrahedron Lett. 1998; 39: 8939
  • 57 Wang M, Li L, Lu J, Luo N, Zhang X, Wang F. Green Chem. 2017; 19: 5172
  • 58 Samanta S, Roy D, Khamarui S, Maiti DK. Chem. Commun. 2014; 50: 2477
  • 59 Kadu VD, Khadul SP, Kothe GJ, Mali GA. Asian J. Org. Chem. 2022; 11: e202200162
  • 60 Adhikary S, Majumder L, Pakrashy S, Srinath R, Mukherjee K, Mandal C, Banerji B. ACS Omega 2020; 5: 14394
  • 61 Gopalaiah K. Chem. Rev. 2013; 113: 3248
  • 62 Darwish M, Wills M. Catal. Sci. Technol. 2012; 2: 243
  • 63 Junge K, Schröder K, Beller M. Chem. Commun. 2011; 47: 4849
  • 64 Correa A, García Mancheño O, Bolm C. Chem. Soc. Rev. 2008; 37: 1108
  • 65 Bolm C. Nat. Chem. 2009; 1: 420
  • 66 Bauer EB. Curr. Org. Chem. 2008; 12: 1341
  • 67 Bolm C, Legros J, Le Paih J, Zani L. Chem. Rev. 2004; 104: 6217
  • 68 Fürstner A. ACS Cent. Sci. 2016; 2: 778
  • 69 Cho SH, Kim JY, Kwak J, Chang S. Chem. Soc. Rev. 2011; 40: 5068
  • 70 Kadu VD. ChemistrySelect 2022; 7: e202104028
  • 71 Tashrifi Z, Khanaposhtani MM, Larijani B, Mahdavi M. Tetrahedron 2021; 84: 131990
  • 72 Alanthadka A, Elango SD, Thangavel P, Subbiah N, Vellaisamy S, Chockalingam UM. Catal. Commun. 2019; 125: 26
  • 73 Kadu VD, Patil AA, Shendage PR. J. Mol. Struct. 2022; 1267: 133502
  • 74 Kadu VD, Chandrudu SN, Hublikar MG, Raut DG, Bhosale RB. RSC Adv. 2020; 10: 23254
  • 75 Zhang Y, Zhang T, Das S. Chem 2022; 8: 3175
  • 76 Gunasekaran N. Adv. Synth. Catal. 2015; 357: 1990
  • 77 Pavithra T, Devi ES, Maheswari CU. Asian J. Org. Chem. 2021; 10: 1861
  • 78 Sterckx H, Morel B, Maes BU. W. Angew. Chem. Int. Ed. 2019; 58: 7946
  • 79 Zhang L.-Y, Wang N.-X, Lucan D, Cheung W, Xing Y. Chem. Eur. J. 2023; 29: e202301700
  • 80 Gopalaiah K, Chandrudu SN. RSC Adv. 2015; 5: 5015
  • 81 Kadu VD, Gund MS, Godage AS. ChemistrySelect 2021; 6: 11954
  • 82 Naróg D, Lechowicz U, Pietryga T, Sobkowiak A. J. Mol. Catal. A: Chem. 2004; 212: 25
  • 83 Rosenau T, Hofinger A, Potthast A, Kosma P. Org. Lett. 2004; 6: 541
  • 84 Yi X, Yi X, Lei S, Liu W, Che F, Yu C, Liu X, Wang Z, Zhou X, Zhang Y. Org. Lett. 2020; 22: 4583
  • 85 Zhang E, Tian H, Xu S, Yu X, Xu Q. Org. Lett. 2013; 15: 2704