Synthesis 2020; 52(19): 2841-2856
DOI: 10.1055/s-0040-1707865
paper
© Georg Thieme Verlag Stuttgart · New York

Solvent-Controlled Divergent Syntheses of Polycyclic N-Fused Heteroaromatics

Anuradha Dagar
,
Dirgha Raj Joshi
,
Ikyon Kim
College of Pharmacy and Yonsei Institute of Pharmaceutical Sciences, Yonsei University, 85 Songdogwahak-ro, Yeonsu-gu, Incheon 21983, Republic of Korea   Email: ikyonkim@yonsei.ac.kr
› Author Affiliations
National Research Foundation of Korea (NRF-2017R1A2A2A05069364, NRF-2018R1A6A1A03023718, and NRF-2020R1A2C2005961)
Further Information

Publication History

Received: 07 April 2020

Accepted after revision: 13 May 2020

Publication Date:
16 June 2020 (online)


Abstract

Due to a growing interest in aza-fused polyaromatic systems among various sciences, enormous attention has been continuously paid to design and synthesize novel chemotypes of N-fused hetero­cycles. During the course of continued efforts in this line, it was found that divergent access to new polycyclic N-fused heteroaromatics was enabled by choice of reaction solvent. Described herein are solvent-controlled selective approaches to three novel N-fused azacycles, benzo-[d]imidazole-pyrrolo[1,2-a]pyrazine hybrids, under mild conditions. The plausible reaction mechanism for each class of compound is suggested as well.

Supporting Information

 
  • References

    • 1a Kwong R, Lam ST, Lee CH. Patent US 20140332758 A1 20141113, 2014
    • 1b Moon D.-H, Lee Y.-G. Patent WO 2018110930 A1 20180621, 2018
    • 1c Damien J. Patent WO 2019115446 A1 20190620, 2019
    • 2a Draper SM, Gregg DJ, Madathil R. J. Am. Chem. Soc. 2002; 124: 3486
    • 2b Delcamp JH, Yella A, Holcombe TW, Nazeeruddin MK, Grätzel M. Angew. Chem. Int. Ed. 2013; 52: 376
    • 2c Takase M, Narita T, Fujita W, Asano MS, Nishinaga T, Benten H, Yoza K, Müllen K. J. Am. Chem. Soc. 2013; 135: 8031
    • 2d Tokimaru Y, Ito S, Nozaki K. Angew. Chem. Int. Ed. 2017; 56: 15560
    • 2e Elbert SM, Reinschmidt M, Baumgärtner K, Rominger F, Mastalerz M. Eur. J. Org. Chem. 2018; 532
    • 4a Park S, Jung Y, Kim I. Tetrahedron 2014; 70: 7534
    • 4b Singh DK, Kim I. ARKIVOC 2019; (iii): 8
    • 4c Kim J, Park M, Choi J, Singh DK, Kwon HJ, Kim SH, Kim I. Bioorg. Med. Chem. Lett. 2019; 29: 1350
    • 4d Seo Y, Lee JW, Park S-h, Namkung W, Kim I. Eur. J. Med. Chem. 2020; 188: 111988
    • 4e Dagar A, Seo Y, Namkung W, Kim I. Org. Biomol. Chem. 2020; 18: 3324
  • 5 Bae GH, Kim S, Lee NK, Dagar A, Lee JH, Lee J, Kim I. RSC Adv. 2020; 10: 7265
  • 6 Dagar A, Bae GH, Lee JH, Kim I. J. Org. Chem. 2019; 84: 6916
  • 7 CCDC 1965113 contains the supplementary crystallographic data for compound 3a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/getstructures.
  • 8 CCDC 1965115 contains the supplementary crystallographic data for compound 4a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/getstructures.
  • 9 CCDC 1965116 contains the supplementary crystallographic data for compound 6a. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/getstructures.

    • For recent examples, see:
    • 10a Kim J, Golime G, Kum HY, Oh K. Asian J. Org. Chem. 2019; 8: 1674
    • 10b Duan X, Liu X, Cuan X, Wang L, Liu K, Zhou H, Chen X, Li H, Wang J. J. Org. Chem. 2019; 84: 12366
    • 10c Yang W.-W, Chen L.-L, Chen P, Ye Y.-F, Wang Y.-B, Zhang X. Chem. Commun. 2020; 56: 1183
    • 11a Bindra AP, Elix JA. Tetrahedron 1969; 25: 3789
    • 11b Perumal S, Mariappan S, Selvaraj S. ARKIVOC 2004; (viii): 46
    • 11c Cano NH, Uranga JG, Nardi M, Procopio A, Wunderlin DA, Santiago AN. Beilstein J. Org. Chem. 2016; 12: 2410
    • 11d Senapak W, Saeeng R, Jaratjarronphong J, Promarak V, Sirion U. Tetrahedron 2019; 75: 3543

      For some recent metal-catalyzed allylic or benzylic oxidations, see:
    • 12a Miller RA, Humphrey GR. Tetrahedron Lett. 1996; 37: 3429
    • 12b Sharma AS, Kaur H. ChemistrySelect 2017; 2: 10112
    • 12c Li S, Zhu B, Lee R, Qiao B, Jiang Z. Org. Chem. Front. 2018; 5: 380
    • 12d Yu H, Zhao Q, Wei Z, Wu Z, Li Q, Han S, Wei Y. Chem. Commun. 2019; 55: 7840
    • 12e Ehudin MA, Quist DA, Karlin KD. J. Am. Chem. Soc. 2019; 141: 12558