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Synthesis 2018; 50(20): 4113-4123
DOI: 10.1055/s-0037-1609585
DOI: 10.1055/s-0037-1609585
paper
Iodine-Promoted C(sp 2)–H Thiolation of Maleimides with Dimethyl Sulfoxide and Thiols
We acknowledge the financial support from Shanghai Municipal Natural Science Foundation (No. 15ZR1401400) and Advanced Organic Chemistry Experimental Reform Foundation (17T10513).Further Information
Publication History
Received: 12 June 2018
Accepted after revision: 21 June 2018
Publication Date:
30 July 2018 (online)

§ Hong-Ru Tan and Lun Wang contributed equally to this work.
Abstract
Iodine-promoted C(sp 2)–H methylthiolation of maleimides using DMSO as synthon has been developed to afford 3-methylthiomaleimides in moderate yields under metal-free conditions. In addition, 3-thiomaleimides were synthesized from maleimides and thiols in the presence of iodine and triethylamine. The methods are simple and efficient for the formation of C–S bond.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1609585.
- Supporting Information
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References
- 1a Robin MP. Wilson P. Mabire AB. Kiviaho JK. Raymond JE. Haddleton DM. Reilly RK. J. Am. Chem. Soc. 2013; 135: 2875
- 1b Smith ME. B. Schumacher FF. Ryan CP. Lauren M. Tedaldi LM. Papaioannou D. Waksman G. Caddick S. Baker JR. J. Am. Chem. Soc. 2010; 132: 1960
- 1c Wang H. Xu M. Xiong MH. Cheng JJ. Chem. Commun. 2015; 51: 4807
- 1d Lázár L. Nagy M. Borbás A. Herczegh P. Zsuga M. Kéki S. Eur. J. Org. Chem. 2015; 7675
- 2a Tang ZC. Wilson P. Kempe K. Chen H. Haddleton DM. Macro Lett. 2016; 5: 709
- 2b Robin MP. O’Reilly RK. Chem. Sci. 2014; 5: 2717
- 2c Jones MW. Strickland RA. Schumacher FF. Caddick S. Baker JR. Gibsona MI. Haddleton DM. Chem. Commun. 2012; 48: 4064
- 3a Csávás M. Miskovics A. Szűcs Z. Rőth E. Nagy ZL. Bereczki I. Herczeg M. Batta G. Nikodém EN. Ostorházi E. Rozgonyi F. Borbás A. Herczegh P. J. Antibiot. 2015; 68: 579
- 3b Castaneda L. Maruani A. Schumacher FF. Miranda E. Chudasama V. Chester KA. Baker JR. Smith ME. B. Caddick S. Chem. Commun. 2013; 49: 8187
- 3c Ashraf SA. Hill J. Zerizer H. Tetrahedron 1992; 48: 6747
- 4a Yoshio I. Keisuke Y. Chiharu N. Japanese Patent JP04149173A, 1992
- 4b Igarashi Y. Watanabe N. Fujita T. Sakamoto M. Watanabe S. Nippon Kagaku Kaishi 1993; 1198
- 4c Igarashi Y. Watanabe S. Nippon Kagaku Kaishi 1990; 1284
- 4d Tominaga Y. Shigemitsu Y. Sasaki K. J. Heterocycl. Chem. 2002; 39: 571
- 4e Kazuo M. Osamu W. Taichiro S. Japanese Patent JP 49016866 B, 1974
- 5a Eichman CC. Stambuli JP. J. Org. Chem. 2009; 74: 4005
- 5b Li YM. Li XY. Wang HF. Chen T. Xie YS. Synthesis 2010; 3602
- 5c Zhang XY. Zhang XY. Guo SR. J. Sulfur Chem. 2011; 32: 23
- 5d Shi YH. Cai ZY. Peng Y. Shi Z. Pang GS. J. Chem. Res. 2011; 35: 161
- 5e Rezaei N. Movassagh B. Tetrahedron Lett. 2016; 57: 1625
- 5f Yu Y. Thom I. Kim SH. Chen DT. Beyer A. Bonnamour J. Zuidema E. Chang S. Bolm C. Adv. Synth. Catal. 2010; 352: 2892
- 6a Fukuzawa S. Shimizu E. Atsuumi Y. Haga M. Ogata K. Tetrahedron Lett. 2009; 50: 2374
- 6b Zheng ZS. Qi DY. Shi L. Catal Commun. 2015; 66: 83
- 6c Ranjit S. Lee R. Heryadi D. Shen C. Wu JE. Zhang PF. Huang KW. Liu XG. J. Org. Chem. 2011; 76: 8999
- 6d Dai C. Xu ZQ. Huang F. Yu ZK. Gao YF. J. Org. Chem. 2012; 77: 4414
- 7a Duan ZY. Ranjit S. Zhang PF. Liu XG. Chem. Eur. J. 2009; 15: 3666
- 7b Ranjit S. Duan ZY. Zhang PF. Liu XG. Org. Lett. 2010; 12: 4134
- 7c Becht JM. Drian CL. J. Org. Chem. 2011; 76: 6327
- 7d Wang PF. Wang XQ. Dai JJ. Feng YS. Xu HJ. Org. Lett. 2014; 16: 4586
- 8 Ravi C. Mohan DC. Adimurthy S. Org. Biomol. Chem. 2016; 14: 2282
- 9 Bagdi AK. Mitra S. Ghosh M. Hajra A. Org. Biomol. Chem. 2015; 13: 3314
- 10 Xiao FH. Xie H. Liu SW. Deng GJ. Adv. Synth. Catal. 2014; 356: 364
- 11 Li X. Li H. Yang W. Zhuang J. Li H. Wang W. Tetrahedron Lett. 2016; 57: 2660
- 12 Chen X. Hao XS. Goodhue CE. Yu JQ. J. Am. Chem. Soc. 2006; 128: 6790
- 13 Chu LL. Yue XY. Qing FL. Org. Lett. 2010; 12: 1644
- 14a Dai C. Xu ZQ. Huang F. Yu ZK. Gao YF. J. Org. Chem. 2012; 77: 4414
- 14b Patil SM. Kulkarni S. Mascarenhas M. Sharma R. Roopan SM. Roychowdhury A. Tetrahedron 2013; 69: 8255
- 14c Ravi C. Mohan DC. Adimurthy S. Org. Biomol. Chem. 2016; 14: 2282
- 14d Xu YF. Cong TT. Liu P. Sun PP. Org. Biomol. Chem. 2015; 13: 9742
- 14e Sharma P. Rohilla S. Jain N. J. Org. Chem. 2015; 80: 4116
- 14f Zou JF. Huang WS. Li L. Xu Z. Zheng ZJ. Yanga KF. Xu LW. RSC Adv. 2015; 5: 30389
- 15a Luo F. Pan CD. Li LP. Chen F. Cheng J. Chem. Commun. 2011; 47: 5304
- 15b Joseph PJ. A. Priyadarshini S. Kantam ML. Sreedhar B. Tetrahedron 2013; 69: 8276
- 15c Mensah EJ. Magolan J. Tetrahedron Lett. 2014; 55: 5323
- 15d Ghosh K. Ranjit S. Mal D. Tetrahedron Lett. 2015; 56: 5199
- 16a Liu FL. Chen JR. Zou YQ. Wei Q. Xiao WJ. Org. Lett. 2014; 16: 3768
- 16b Li HY. Xing LJ. Lou MM. Wang H. Liu RH. Wang B. Org. Lett. 2015; 17: 1098
- 17 Shukla G. Srivastava A. Nagaraju A. Raghuvanshi K. Singh MS. Adv. Synth. Catal. 2015; 357: 3969
- 18 Shen T. Huang XQ. Liang YF. Jiao N. Org. Lett. 2015; 17: 6186
- 19 Jiang X. Wang C. Wei YW. Xue D. Liu ZT. Xiao JL. Chem. Eur. J. 2014; 20: 58
- 20 Mahajan PS. Tanpure SD. More NA. Gajbhiye JM. Mhaske SB. RSC Adv. 2015; 5: 101641
- 21 Fei HY. Yu JT. Jiang Y. Guo H. Cheng J. Org. Biomol. Chem. 2013; 11: 7092
- 22 Ren XY. Chen JB. Chen F. Cheng J. Chem. Commun. 2011; 47: 6725
- 23 Jiang Y. Loh TP. Chem. Sci. 2014; 5: 4939
- 24a Gao XF. Pan XJ. Gao J. Jiang HF. Yuan GQ. Li YW. Org. Lett. 2015; 17: 1038
- 24b Gao XF. Pan XJ. Gao J. Huang HW. Yuan GQ. Li YW. Chem. Commun. 2015; 51: 210
- 24c Gao QH. Wu X. Li YH. Liu S. Meng XG. Wu AX. Adv. Synth. Catal. 2014; 356: 2924
- 25a Yang ZH. An YL. Chen Y. Shao ZY. Zhao SY. Adv. Synth. Catal. 2016; 358: 3869
- 25b Yang ZH.. Tan H. R. An YL. Zhao YW. Lin HP. Zhao SY. Adv. Synth. Catal. 2018; 360: 173
- 25c An YL. Yang ZH. Zhang HH. Zhao SY. Org. Lett. 2016; 18: 152
- 25d An YL. Deng YX. Zhang W. Zhao SY. Synthesis 2015; 47: 1581
- 26a Arai Y. Matsui M. Koizumi T. Shiro M. J. Org. Chem. 1991; 56: 1983
- 26b Barry JF. Wallace TW. Walshe ND. A. Tetrahedron 1995; 51: 12797
- 27a Uno BE. Deibler KK. Villa C. Raghuraman A. Scheidt KA. Adv. Synth. Catal. 2018; 360: 1719
- 27b Chalker JM. Bernardes GJ. L. Lin YA. Davis BG. Chem. Asian J. 2009; 4: 630
- 28a Liu X. Cui H. Yang D. Dai S. Zhang G. Wei W. Wang H. Catal. Lett. 2016; 146: 1743
- 28b Choudhury P. Roy B. Basu B. Asian J. Org. Lett. 2017; 6: 1569
- 28c Parumala SK. R. Peddinti RK. Green Chem. 2015; 17: 4068
- 28d Siddaraju Y. Prabhu KR. Org. Lett. 2016; 18: 6090
- 29 White JE. J. Polym. Sci., Polym. Chem. 1987; 25: 1191
- 30 Sahoo MK. Mhaske SB. Argade NP. Synthesis 2003; 346
- 31 Sammut IA. Harrison JC. Hewitt RJ. Read MI. Stanley NJ. Woods LM. Kueh JT. B. Jay-Smith M. Smith RA. J. Giles G. Larsen L. Rennison D. Brimble MA. Larsen DS. Patent WO 2017095237, 2017