CC BY 4.0 · SynOpen 2023; 07(02): 154-160
DOI: 10.1055/s-0042-1751451
letter

Highly Efficient Synthesis of 3,3-Disubstituted Oxindoles through Direct Oxidative Alkylarylation of N-Arylacrylamides with Simple Alkanes

Yan Chen
a   Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, Zhejiang, P. R. of China
,
Weihong Song
b   College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou, 311121, P. R. of China
,
Zhixiang Zhou
a   Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, Zhejiang, P. R. of China
,
Ziye Zhang
a   Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, Zhejiang, P. R. of China
,
Kai Liu
a   Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, Zhejiang, P. R. of China
,
Xiaofei Zeng
b   College of Material, Chemistry and Chemical Engineering, Hangzhou Normal University, Hangzhou, 311121, P. R. of China
,
Xiaoyu Han
a   Zhejiang Provincial Key Laboratory for Chemical & Biological Processing Technology of Farm Products School of Biological & Chemical Engineering, Zhejiang University of Science and Technology, Hangzhou 310023, Zhejiang, P. R. of China
› Author Affiliations
We gratefully acknowledge the Basic Public Welfare Research Program of Zhejiang Province (LGJ22B020001) for generous financial support.


Abstract

A direct oxidative alkylarylation reaction of N-arylacrylamides with simple alkanes for the synthesis of 3,3-disubstituted oxindoles under metal-free conditions was demonstrated. By using PhI(OAc)2 [(diacetoxy)iodobenzene] as an oxidant, a series of 3,3-disubstituted oxindoles bearing different aryl or alkyl substituents were generated in moderate to excellent chemical yields via a radical-initiated alkylation/cyclization process. The reported method features good functional group tolerance and wide substrate range, and provides an effective method for the preparation of various alkyl substituted 3,3-disubstituted oxindoles.

Supporting Information



Publication History

Received: 26 January 2023

Accepted after revision: 20 April 2023

Article published online:
08 May 2023

© 2023. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by/4.0/)

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

 
  • References and Notes


    • For recent reviews, see:
    • 1a Khetmails YM, Shivani M, Murugesan S, Sekhar KV. G. C. Biomed. Pharmacother. 2021; 141: 111842
    • 1b Mermer A, Keles T, Sirin Y. Bioorg. Chem. 2021; 114: 105076
    • 1c Wang Y, Yang M, Sun YY, Wu ZG, Dai H, Li S. Org. Lett. 2021; 23: 8750
    • 1d Christodoulou MS, Nicoletti F, Mangano K, Chiacchio MA, Facchetti G, Rimoldi I, Beccalli EM, Giofrè S. Bioorg. Med. Chem. Lett. 2020; 30: 126845
    • 1e Wang C, Liu L. Org. Chem. Front. 2021; 8: 1454
    • 1f Cao ZY, Zhou F, Zhou J. Acc. Chem. Res. 2018; 51: 1443
    • 2a Wang X, Zhong Y, Mo Z, Wu S, Xu Y, Tang H, Pan Y. Adv. Synth. Catal. 2021; 363: 20
    • 2b Che F, Zhong J, Yu L, Ma C, Yu C, Wang M, Hou Z, Zhang Y. Adv. Synth. Catal. 2020; 362: 5020
    • 2c Wang Y, Lin W, Zou J, Yu W, Liu X. Adv. Synth. Catal. 2020; 362: 3116
    • 2d Majhi J, Granados A, Matsuo B, Ciccone V, Dhungana RK, Sharique M, Molander GA. Chem. Sci. 2023; 14: 897
    • 2e Radhoff N, Studer A. Chem. Sci. 2022; 13: 3875
    • 2f Xu J, Liang L, Zheng H, Chi YR, Tong R. Nat. Commun. 2019; 10: 4754
    • 2g Gajulapalli VP. R, Kumarswamyreddy N, Lokesh K, Kesavan V. ChemistrySelect 2021; 6: 7855
    • 2h Chen J, Cai Y, Zhao G. Adv. Synth. Catal. 2014; 356: 359
    • 2i He ZY, Guo JY, Tian SK. Adv. Synth. Catal. 2018; 360: 1544
    • 2j Liu WK, Wang BL, Zhou SS, Shen JH, Wang Z, Wang XW. Org. Lett. 2023; 25: 104
    • 3a Su Y, Cao L, Shi Y, Feng Y, Xue W, Cao G, Wang KH, Huang D, Huo C, Hu Y. Synthesis 2019; 51: 2331
    • 3b Liu Z, Zhong S, Ji X, Deng GJ, Huang H. ACS Catal. 2021; 11: 4422
    • 3c Gui Q, Hu L, Chen X, Liu J, Tan Z. Asian J. Org. Chem. 2015; 4: 870
    • 3d Li X, Han MY, Wang B, Wang L, Wang M. Org. Biomol. Chem. 2019; 17: 6612
    • 3e Fan X, Liu H, Ma S, Wang F, Yang J, Li D. Tetrahedron 2022; 117: 132849
    • 3f Su L, Xue P, Zhu X, Sun H, Liu J, Wang C. J. Org. Chem. 2022; 87: 874
    • 3g Li X, Han MY, Wang B, Wang L, Wang M. Org. Biomol. Chem. 2019; 17: 6612
    • 3h Sun Z, Huang H, Wang Q, Huang C, Mao G, Deng GJ. Org. Chem. Front. 2022; 9: 3506

      For recent reviews, see:
    • 4a Sun K, Lv QY, Lin YW, Yu B, He WM. Org. Chem. Front. 2021; 8: 445
    • 4b Liao J, Yang X, Ouyang L, Lai Y, Huang J, Luo R. Org. Chem. Front. 2021; 8: 1345
    • 4c Wang W, Zhang M, Yang W, Yang X. Chin. J. Org. Chem. 2022; 42: 75
    • 4d Zhai S, Qiu S, Yang S, Hua B, Niu Y, Han C, Yu Y, Li Y, Zhai H. Chin. Chem. Lett. 2022; 33: 276
    • 4e Zhang J, Liu P, Sun P. Chin. J. Org. Chem. 2021; 41: 185
    • 5a Zeng FL, Xie KC, Liu YT, Wang H, Yin PC, Qu LB, Chen XL, Yu B. Green Chem. 2022; 24: 1732
    • 5b Gui QW, Teng F, Li ZC, Xiong ZY, Jin XF, Lin YW, Cao Z, He WM. Chin. Chem. Lett. 2021; 32: 1907
    • 5c Qu Z, Tian T, Tan Y, Ji X, Deng GJ, Huang H. Green Chem. 2022; 24: 7403
    • 5d Wang QL, Zhou Q, Liao J, Chen Z, Xiong BQ, Deng GJ, Tang KW, Liu Y. J. Org. Chem. 2021; 86: 2866
    • 5e Ding S, Ren H, Zhu M, Ma Q, Miao Z, Li P. Synth. Commun. 2021; 51: 593
    • 5f Weng J, Pan L, Yao P, Feng Y, Fu W. Appl. Organomet. Chem. 2021; 35: 6366
    • 5g Xu Z, Jia R, Ma Z, Cao S, Shen L, Ji H. Synlett 2019; 30: 1909
    • 5h Zhang MZ, Li WT, Li YY, Wang Q, Li C, Liu YH, Yin JX, Yang X, Huang H, Chen T. J. Org. Chem. 2021; 86: 15544
    • 5i Yang Z, Tang A. Synlett 2019; 30: 1061
    • 5j Muralirajan K, Kancherla R, Gimnkhan A, Rueping M. Org. Lett. 2021; 23: 6905
    • 5k Kong W, Casimiro M, Fuentes N, Merino E, Nevado C. Angew. Chem. Int. Ed. 2013; 52: 13086
    • 6a Lu MZ, Loh TP. Org. Lett. 2014; 16: 4698
    • 6b Chen H, Sun Z, Yang H, Mao F, Yan X, Li X, Xu X. Synlett 2022; 34: 63
    • 7a Ji PY, Zhang MZ, Xu JW, Liu YF, Guo CC. J. Org. Chem. 2016; 81: 5181
    • 7b Sun X, Zhu JP, Qiu QC, He YL, Hu DR, Li XL, Lu GP, Yuan YH, Zhang XF, Xu X, Yu M, Hu B. Org. Biomol. Chem. 2022; 20: 8042
    • 8a Sakamoto R, Hirama N, Maruoka K. Org. Biomol. Chem. 2018;
    • 8b Jia F, Liu K, Xi H, Lu S, Li Z. Tetrahedron Lett. 2013; 54: 6337
    • 8c Biswas P, Paul S, Guin J. Angew. Chem. Int. Ed. 2016; 55: 7756
    • 8d Zhou MB, Song RJ, Ouyang XH, Liu Y, Wei WT, Deng GB, Li JH. Chem. Sci. 2013; 4: 2690
  • 9 Yu WQ, Fan JH, Chen P, Xiong BQ, Xie J, Tang KW, Liu Y. Org. Biomol. Chem. 2022; 20: 1958
  • 10 Wang H, Guo LN, Duan XH. Org. Lett. 2013; 15: 5254
    • 12a Li X, Xu J, Gao Y, Fang H, Tang G, Zhao Y. J. Org. Chem. 2015; 80: 2621
    • 12b Li X, Han MY, Wang B, Wang L, Wang M. Org. Biomol. Chem. 2019; 17: 6612
    • 13a Wu T, Mu X, Liu G. Angew. Chem. Int. Ed. 2011; 50: 12578
    • 13b Pan C, Zhang H, Zhu C. Org. Biomol. Chem. 2015; 13: 361
    • 13c Wu T, Mu X, Liu G. Angew. Chem. Int. Ed. 2011; 50: 12578
    • 13d Zhao Y, Li Z, Sharma U, Sharma N, Song G, Eycken EV. Chem. Commun. 2016; 52: 6395
  • 14 Yi H, Zhang G, Wang H, Huang Z, Wang J, Singh AK, Lei A. Chem. Rev. 2017; 117: 9016
  • 15 Li ZJ, Zhang Y, Zhang LZ, Liu ZQ. Org. Lett. 2014; 16: 382
    • 16a Iyer A, Jockusch S, Sivaguru J. J. Phys. Chem. A 2014; 118: 10596
    • 16b Yuan Y, Shen T, Wang K, Jiao N. Chem. Asian J. 2013; 8: 2932