Abstract
The heterocyclic mesoionic compound (1,4-diphenyl-1H-1,2,4-triazol-4-ium-3-yl)(phenyl)amide („Nitron“) has recently been found to exist in a prototropic equilibrium with minor amounts of a nucleophilic heterocyclic carbene of the 1,2,4-triazolyl-5-ylidene type. Here we report that Nitron reacts with 1-trifluoromethyl-substituted prop-2-yne iminium salts by conjugate nucleophilic addition of the anionic PhN‒ substituent in the mesoionic tautomer, whereas the nucleophilic triazolylidene form is involved in the reaction with 1-CF3-prop-2-yne imines. 3-(2,3-Dihydro-1H-benzo[c]azepin-5-yl)-1H-1,2,4-triazol-4-ium triflate salts were obtained in the former case and (Z)-9-arylidene-1,2,4,7-tetraazaspiro[4.4]nona-2,7-dienes in the latter.
Acknowledgments
We thank B. Müller (Institute of Inorganic Chemistry II) for the collection of the X-ray diffraction data and Dr. M. Wunderlin for obtaining the mass spectra.
Author contribution: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: Ulm University.
Conflict of interest statement: The authors declare no conflicts of interest regarding this article.
References
1. The Merck Index: An Encyclopaedia of Chemicals, Drugs and Biologicals, 13th ed.; Merck & Co., Inc.: Whitehouse Station, New Jersey, 2001. entry 6646.Suche in Google Scholar
2. Busch, M. Ber. Dtsch. Chem. Ges. 1905, 38, 856–860; https://doi.org/10.1002/cber.190503801148.Suche in Google Scholar
3. Busch, M. Ber. Dtsch. Chem. Ges. 1905, 38, 861–866; https://doi.org/10.1002/cber.190503801149.Suche in Google Scholar
4. Schönberg, A. J. Chem. Soc. 1938, 824–825; https://doi.org/10.1039/jr9380000824.Suche in Google Scholar
5. Warren, F. L. J. Chem. Soc. 1938, 1100.Suche in Google Scholar
6. Baker, W., Ollis, W. D. Q. Rev. 1957, 11, 15–29; https://doi.org/10.1039/qr9571100015.Suche in Google Scholar
7. Olah, G. A. J. Inorg. Nucl. Chem. 1961, 16, 225–232; https://doi.org/10.1016/0022-1902(61)80494-6.Suche in Google Scholar
8. X-ray structure determination, Cannon, J. R., Raston, C. L., White, A. H. Aust. J. Chem. 1980, 33, 2237–2247; https://doi.org/10.1071/ch9802237.Suche in Google Scholar
9. Simas, A. M., Miller, J., de Athayade Filho, P. F. Can. J. Chem. 1998, 76, 869–872; https://doi.org/10.1139/v98-065.Suche in Google Scholar
10. Ramsden, C. A., Oziminski, W. P. Tetrahedron 2015, 71, 6846–6851; https://doi.org/10.1016/j.tet.2015.07.024.Suche in Google Scholar
11. Färber, C., Leibold, M., Bruhn, C., Maurer, M., Siemeling, U. Chem. Commun. 2012, 48, 227–229; https://doi.org/10.1039/c1cc16460k.Suche in Google Scholar PubMed
12. Hitzel, S., Färber, C., Bruhn, C., Siemeling, U. Organometallics 2014, 33, 425–428; https://doi.org/10.1021/om401058e.Suche in Google Scholar
13. Thie, C., Hitzel, S., Wallbaum, L., Bruhn, C., Siemeling, U. J. Organomet. Chem. 2016, 821, 112–121; https://doi.org/10.1016/j.jorganchem.2016.03.023.Suche in Google Scholar
14. Enders, D., Breuer, K., Raabe, G., Runsink, J., Teles, J. H., Melder, J.-P., Ebel, K., Brode, S. Angew. Chem. Int. Ed. Engl. 1995, 34, 1021–1023; https://doi.org/10.1002/anie.199510211.Suche in Google Scholar
15. Enders, D., Breuer, K., Runsink, J., Teles, J. H. Liebigs Ann. Chem. 1996, 2019–2028; https://doi.org/10.1002/jlac.199619961212.Suche in Google Scholar
16. Enders, D., Breuer, K., Kallfass, U., Balensiefer, T. Synthesis 2003, 1292–1295; https://doi.org/10.1055/s-2003-39409.Suche in Google Scholar
17. Reisser, M., Maas, G. J. Org. Chem. 2004, 69, 4913–4924; https://doi.org/10.1021/jo049586o.Suche in Google Scholar PubMed
18. Espenlaub, S., Gerster, H., Maas, G. ARKIVOC 2007, (iii), 114–131; https://doi.org/10.3998/ark.5550190.0008.311.Suche in Google Scholar
19. Schneider, T., Seitz, B., Schiwek, M., Maas, G. J. Fluor. Chem. 2020, 235, 109567; https://doi.org/10.1016/j.jfluchem.2020.109567.Suche in Google Scholar
20. Schneider, T., Keim, M., Seitz, B., Maas, G. Beilstein J. Org. Chem. 2020, 16, 2064–2072; https://doi.org/10.3762/bjoc.16.173.Suche in Google Scholar PubMed PubMed Central
21. Weil, M., Fürst, M. Acta Crystallogr. 2020, E76, 1003–1006; https://doi.org/10.1107/s2056989020006933.Suche in Google Scholar
22. Reinhard, R., Glaser, M., Neumann, R., Maas, G. J. Org. Chem. 1997, 62, 7744–7751; https://doi.org/10.1021/jo9710036.Suche in Google Scholar
23. Nedolya, N. A., Trofinov, B. A. Chem. Heterocycl. Compd. 2013, 49, 152–176. translated from: Khim. Geterosikl. Soedin. 2013, 49, 166‒190; https://doi.org/10.1007/s10593-013-1236-y.Suche in Google Scholar
24. Chen, Z., Zhu, J., Xie, H., Li, S., Wu, Y., Gong, Y. Org. Biomol. Chem. 2011, 9, 5682–5691; https://doi.org/10.1039/c1ob05371j.Suche in Google Scholar PubMed
25. Johnson, P. L., Renga, J. M., Galliford, C. V., Whiteker, G. T., Giampietro, N. C. Org. Lett. 2015, 17, 2905–2907; https://doi.org/10.1021/acs.orglett.5b01176.Suche in Google Scholar PubMed
26. Cao, J., Yang, X., Hua, Y., Deng, Y., Lai, G. Org. Lett. 2011, 13, 478–481; https://doi.org/10.1021/ol1028207.Suche in Google Scholar PubMed
27. Chen, J.-R., Hu, X.-Q., Lu, L.-Q., Xiao, W.-J. Chem. Rev. 2015, 115, 5301−5365; https://doi.org/10.1021/cr5006974.Suche in Google Scholar PubMed
28. Grant, J. A., Lu, Z., Tucker, D. E., Hockin, B. M., Yufit, D. S., Fox, M. A., Kataky, R., Chechik, V., O’Donoghue, A. C. Nat. Commun. 2017, 8, 15088; https://doi.org/10.1038/ncomms15088.Suche in Google Scholar PubMed PubMed Central
29. Sheldrick, G. M. Acta Crystallogr. 2008, A64, 112–122; https://doi.org/10.1107/s0108767307043930.Suche in Google Scholar PubMed
30. Sheldrick, G. M. Acta Crystallogr. 2015, C71, 3–8.Suche in Google Scholar
31. Farrugia, L. J. J. Appl. Crystallogr. 2012, 45, 849–854; https://doi.org/10.1107/s0021889812029111.Suche in Google Scholar
Supplementary Material
The online version of this article offers supplementary material (https://doi.org/10.1515/znb-2020-0178).
© 2020 Walter de Gruyter GmbH, Berlin/Boston
Artikel in diesem Heft
- Frontmatter
- In this issue
- Research Articles
- A zinc(II) coordination polymer based on a flexible bis(benzimidazole) ligand: synthesis, crystal structure and fluorescence study
- A study of antituberculosis activities and crystal structures of (E)-2-[2-(arylidene)hydrazinyl]pyrimidine and (E)-N1-(arylidene)pyrimidine-2-carbohydrazide derivatives
- Pt3Ni/C and Pt3Co/C cathodes as electrocatalysts for use in oxygen sensors and proton exchange membrane fuel cells
- Selective cyclization modes of methyl 3′-heteroarylamino-2′-(2,5-dichlorothiophene-3-carbonyl)acrylates. Synthesis of model (thienyl)pyrazolo- and triazolo[1,5-α]pyrimidines
- Synthesis and crystal structures of two new lead(II) complexes with the pincer-type ligand 4′-(4-chlorophenyl)-2,2′:6′,2″-terpyridine (Cl-Ph-tpy): subtle interplay of weak intermolecular interactions
- Die unerwartete Kristallstruktur des Cäsium-Dodekahydro-Monocarba-closo-Dodekaborats Cs[CB11H12]
- Synthesis, crystal structure and photoluminescence of a binuclear rhenium(I) carbonyl complex incorporated in a framework of a distorted salophen ligand
- 1-Trifluoromethyl-prop-2-yne 1-iminium salts and 1-imines: reactions with the mesoionic „Nitron“
- Note
- YIrIn with ZrNiAl-type structure
Artikel in diesem Heft
- Frontmatter
- In this issue
- Research Articles
- A zinc(II) coordination polymer based on a flexible bis(benzimidazole) ligand: synthesis, crystal structure and fluorescence study
- A study of antituberculosis activities and crystal structures of (E)-2-[2-(arylidene)hydrazinyl]pyrimidine and (E)-N1-(arylidene)pyrimidine-2-carbohydrazide derivatives
- Pt3Ni/C and Pt3Co/C cathodes as electrocatalysts for use in oxygen sensors and proton exchange membrane fuel cells
- Selective cyclization modes of methyl 3′-heteroarylamino-2′-(2,5-dichlorothiophene-3-carbonyl)acrylates. Synthesis of model (thienyl)pyrazolo- and triazolo[1,5-α]pyrimidines
- Synthesis and crystal structures of two new lead(II) complexes with the pincer-type ligand 4′-(4-chlorophenyl)-2,2′:6′,2″-terpyridine (Cl-Ph-tpy): subtle interplay of weak intermolecular interactions
- Die unerwartete Kristallstruktur des Cäsium-Dodekahydro-Monocarba-closo-Dodekaborats Cs[CB11H12]
- Synthesis, crystal structure and photoluminescence of a binuclear rhenium(I) carbonyl complex incorporated in a framework of a distorted salophen ligand
- 1-Trifluoromethyl-prop-2-yne 1-iminium salts and 1-imines: reactions with the mesoionic „Nitron“
- Note
- YIrIn with ZrNiAl-type structure