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DOI: 10.1055/a-2580-6573
Synthesis of Pyrazolines via (3+2) Cycloaddition of Nitrile Imines and N-Silyl Enamines
This work was supported by a research grant from Inha University.

Abstract
The synthesis of tricyclic fused pyrazolines from N-silyl enamines and nitrile imines is presented. N-Silyl enamines are an emerging class of enamines that can be used as free enamine surrogates. The N-silyl enamines, prepared from readily available isoquinolines, underwent (3+2) cycloaddition with a wide range of nitrile imines to form the corresponding pyrazolines in moderate to good yields. This cascade protocol entailed the in situ utilization of both N-silyl enamine and nitrile imine intermediates.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-2580-6573.
- Supporting Information
Publikationsverlauf
Eingereicht: 28. Februar 2025
Angenommen nach Revision: 10. April 2025
Accepted Manuscript online:
10. April 2025
Artikel online veröffentlicht:
08. Mai 2025
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References
- 1a Byrd JC, Furman RR, Coutre SE, Flinn IW, Burger JA, Blum KA, Grant B, Sharman JP, Coleman M, Wierda WG, Jones JA, Zhao W, Heerema NA, Johnson AJ, Sukbuntherng J, Chang BY, Clow F, Hedrick E, Buggy JJ, James DF, O’Brien SN. Engl. J. Med. 2013; 369: 32
- 1b El-Sherief HA. M, Youssif BG. M, Abbas Bukhari SN, Abdelazeem AH, Abdel-Aziz M, Abdel-Rahman HM. Eur. J. Med. Chem. 2018; 156: 774
- 1c Shaaban MR, Mayhoub AS, Farag AM. Expert Opin. Ther. Pat. 2012; 22: 253
- 1d Karad SC, Purohit VB, Thakor P, Thakkar VR, Raval DK. Eur. J. Med. Chem. 2016; 112: 270
- 1e Hassan GS, Georgey HH, Mohammed EZ, George RF, Mahmoud WR, Omar FA. Eur. J. Med. Chem. 2021; 218: 113389
- 1f Iñiguez MA, Punzón C, Cacheiro-Llaguno C, Díaz-Muñoz MD, Duque J, Cuberes R, Alvarez I, Andrés EM, Buxens J, Buschmann H, Vela JM, Fresno M. Int. Immunopharmacol. 2010; 10: 1295
- 2a Nehra B, Rulhania S, Jaswal S, Kumar B, Singh G, Monga V. Eur. J. Med. Chem. 2020; 205: 112666
- 2b Matiadis D, Sagnou M. Int. J. Mol. Sci. 2020; 21: 5507
- 2c Haider K, Shafeeque M, Yahya S, Yar MS. Eur. J. Med. Chem. Rep. 2022; 5: 100042
- 3a Matiadis D. Adv. Synth. Catal. 2023; 365: 1934
- 3b Farooq S, Ngaini Z. Tetrahedron Lett. 2020; 61: 151416
- 3c Han S. Bull. Korean Chem. Soc. 2023; 44: 172
- 3d Lee SS, Oh CH. Bull. Korean Chem. Soc. 2024; 45: 759
- 3e Park H, Raikar SS, Ahn MJ, Kim SH, Kim P. Bull. Korean Chem. Soc. 2024; 45: 551
- 4a Campbell NR, Sun B, Singh RP, Deng L. Adv. Synth. Catal. 2011; 353: 3123
- 4b Fernández M, Reyes E, Vicario JL, Badía D, Carrillo L. Adv. Synth. Catal. 2012; 354: 371
- 4c Müller S, List B. Angew. Chem. Int. Ed. 2009; 48: 9975
- 4d Mahé O, Dez I, Levacher V, Brière J.-F. Angew. Chem. Int. Ed. 2010; 49: 7072
- 4e Lv Y, Meng J, Li C, Wang X, Ye Y, Sun K. Adv. Synth. Catal. 2021; 363: 5235
- 4f Singh V, Mishra BK, Kumar D, Tiwari B. Org. Lett. 2023; 25: 7089
- 4g Chen M, Wang L.-J, Ren P.-X, Hou X.-Y, Fang Z, Han M.-N, Li W. Org. Lett. 2018; 20: 510
- 5a Hu S, Du S, Yang Z, Ni L, Chen Z. Adv. Synth. Catal. 2019; 361: 3124
- 5b Chen J.-R, Dong W.-R, Candy M, Pan F.-F, Jörres M, Bolm C. J. Am. Chem. Soc. 2012; 134: 6924
- 5c Attanasi OA, De Crescentini L, Favi G, Mantellini F, Mantenuto S, Nicolini S. J. Org. Chem. 2014; 79: 8331
- 5d Chen D.-Z, Xiao W.-J, Chen J.-R. Org. Chem. Front. 2017; 4: 1289
- 5e Hu K, Zhang D, Wang S, Lin L, Feng X. Org. Chem. Front. 2023; 10: 2422
- 5f Huang R, Tao H.-Y, Wang C.-J. Org. Lett. 2017; 19: 1176
- 5g Wang Z, Yang Y, Gao F, Wang Z, Luo Q, Fang L. Org. Lett. 2018; 20: 934
- 5h Chen B, Chu W.-D, Liu Q.-Z. RSC Adv. 2019; 9: 1487
- 6a Hashimoto T, Maruoka K. Chem. Rev. 2015; 115: 5366
- 6b Deepthi A, Thomas NV, Sruthi SL. New J. Chem. 2021; 45: 8847
- 6c Nájera C, Sansano JM, Yus M. Org. Biomol. Chem. 2015; 13: 8596
- 7a Su Y, Zhao Y, Chang B, Zhao X, Zhang R, Liu X, Huang D, Wang K.-H, Huo C, Hu Y. J. Org. Chem. 2019; 84: 6719
- 7b Tu L, Gao L, Wang Q, Cao Z, Huang R, Zheng Y, Liu J. J. Org. Chem. 2022; 87: 3389
- 7c Kowalczyk A, Utecht-Jarzyńska G, Mlostoń G, Jasiński M. Org. Lett. 2022; 24: 2499
- 7d Sibi MP, Stanley LM, Jasperse CP. J. Am. Chem. Soc. 2005; 127: 8276
- 7e Wang G, Liu X, Huang T, Kuang Y, Lin L, Feng X. Org. Lett. 2013; 15: 76
- 7f Tu L, Gao L, Wang X, Shi R, Ma R, Li J, Lan X, Zheng Y, Liu J. J. Org. Chem. 2021; 86: 559
- 7g Sibi MP, Stanley LM, Soeta T. Adv. Synth. Catal. 2006; 348: 2371
- 7h Jamieson C, Livingstone K. The Nitrile Imine 1,3-Dipole: Properties, Reactivity and Applications. Springer International Publishing; Cham: 2020
- 8a Dadiboyena S, Hamme AT. II. Eur. J. Org. Chem. 2013; 7567
- 8b Zhou Y, Ma R, Li X, Liu X, Wang K.-H, Wang J, Huang D, Hu Y. J. Org. Chem. 2023; 88: 17356
- 8c Yıldırım M, Dürüst Y. Tetrahedron 2011; 67: 3209
- 8d Liu X, Zhou Y, Li X, Wang K.-H, Wang J, Huang D, Lv X, Hu Y. Tetrahedron 2024; 166: 134241
- 9a Kitane S, Tshiamala K, Laude B, Vebrel J, Ceritti E. Tetrahedron 1985; 41: 3737
- 9b Kitane S, Sebban A, Vebrel J, Laude B. Bull. Soc. Chim. Belg. 1989; 98: 105
- 9c Daou B, Soufiaoui M, Carrié R. J. Heterocycl. Chem. 1989; 26: 1485
- 9d Donohue AC, Pallich S, McCarthy TD. J. Chem. Soc., Perkin Trans. 1 2001; 2817
- 10 Cao VD, Kim H, Kwak J, Joung S. Org. Lett. 2022; 24: 1974
- 11a Park S, Chang S. Angew. Chem. Int. Ed. 2017; 56: 7720
- 11b Gandhamsetty N, Joung S, Park S.-W, Park S, Chang S. J. Am. Chem. Soc. 2014; 136: 16780
- 11c Gandhamsetty N, Park S, Chang S. J. Am. Chem. Soc. 2015; 137: 15176
- 11d Cao V, Jo D, Kim H, Kim C, Yun S, Joung S. Synthesis 2021; 53: 754
- 11e Park S. Chin. J. Chem. 2019; 37: 1057
- 12a Spiteri C, Keeling S, Moses JE. Org. Lett. 2010; 12: 3368
- 12b Garve LK. B, Petzold M, Jones PG, Werz DB. Org. Lett. 2016; 18: 564
- 12c Kowalczyk A, Utecht-Jarzyńska G, Mlostoń G, Jasiński M. J. Fluorine Chem. 2021; 241: 109691
- 12d Lin B, Zhang Z, Yao Y, You Y, Weng Z. Molecules 2022; 27: 6568
- 13 Details are available in the Supporting Information.
- 14 Detailed optimization results are available in the Supporting Information.
- 15 Fasano V, Radcliffe JE, Ingleson MJ. ACS Catal. 2016; 6: 1793