Subscribe to RSS
DOI: 10.1055/s-2007-983834
Synthesis and Structure of Thia and Selena Heterocycles Containing Cycloamidine Substructures
Publication History
Publication Date:
08 August 2007 (online)
Abstract
Cyclization of a bis-arylimidoyl chloride with an acylselenourea leads to the construction of a 1,3-selenazolidine with a heteroradialene structure. Another reaction of the bis-arylimidoyl chloride (hydrazinolysis) leads to the formation of Δ2-1,2-diazetines, which we have shown previously to be reactive precursors for ring transformation reactions that yield unusual heterocycles. We now demonstrate that the reaction of these Δ2-1,2-diazetines with various isothio- or isoselenocyanates affords an efficient entry to highly substituted 1,3,4-thia- or -selenadiazines. The structures of these novel derivatives were confirmed by NMR and mass spectroscopy, elemental analysis, and X-ray structural analysis. Detailed multidimensional 77Se NMR experiments as well as density functional theory (DFT) calculations show structural specifics of these compounds.
Key words
ring expansion - heterocycles - selenium - sulfur - noncovalent chalcogen interactions
-
1a
Schwarz K.Foltz CM. J. Am. Chem. Soc. 1957, 79: 3292 -
1b
Ursini F.Bindoli A. Chem. Phys. Lipids 1987, 44: 255 -
1c
Stadtman T. Annu. Rev. Biochem. 1990, 59: 111 -
1d
Forchhammer K.Böck A. Naturwissenschaften 1991, 78: 497 -
1e
Stadtman T. J. Biol. Chem. 1991, 266: 16257 -
1f
Stadtman T. Annu. Rev. Biochem. 1996, 65: 83 -
2a
Kirsi JJ.McKernan PA.Burns NJ.North JA.Murray BK.Robins RK. Antimicrob. Agents Chemother. 1984, 26: 466 -
2b
Robins RK.Revankar GR.McKernan PA.Murray BK.Kirsi JJ.North JA. Adv. Enzyme Regul. 1985, 24: 29 -
2c
Gebeyehu G.Marquez VE.Van Cott A.Cooney DA.Kelley JA.Jayaram HN.Ahluwalia GS.Dion RL.Wilson YA.Johns DG. J. Med. Chem. 1985, 28: 99 -
2d
Natsumeda Y.Yamada Y.Yamaji Y.Weber G. Biochem. Biophys. Res. Commun. 1988, 153: 321 -
2e
Franchetti P.Cappellacci L.Abu Sheikha G.Jayaram HN.Gurudutt VV.Sint T.Schneider BP.Jones WD.Goldstein BM.Perra G.De Montis A.Loi AG.La Colla P.Grifantini M. J. Med. Chem. 1997, 40: 1731 -
2f
Parker WB. Virus Res. 2005, 107: 165 -
2g
Sarma BK.Mugesh G. J. Am. Chem. Soc. 2005, 127: 15207 -
3a
Shinkai I.Larsen RD. In Comprehensive Heterocyclic Chemistry II Vol. 3: Pergamon; New York: 1996. p.493-510 -
3b
Boulton AJ.Smalley RK.Sainsbury M. In Comprehensive Heterocyclic Chemistry II Vol. 6: Pergamon; New York: 1996. 737-783. p.987-1018 -
3c
Mochowski J.Kloc K.Lisiak R.Potaczek P.Wójtowicz H. Arkivoc 2007, (vi): 14 -
3d
Garud DR.Koketsu M.Ishihara H. Molecules 2007, 12: 504 -
4a
Beckert R.Mayer R. J. Prakt. Chem. 1982, 324: 227 -
4b
Beckert R.Gruner M.Seidel I.Kuban R.-J. Monatsh. Chem. 1989, 120: 1125 -
4c
Beckert R.Gruner M. J. Prakt. Chem. 1990, 332: 65 -
4d
Brandenburg J.Käpplinger C.Beckert R. Synthesis 1996, 1302 -
4e
Brandenburg J.Beckert R.Fehling P.Döring M.Görls H. J. Prakt. Chem./Chem.-Ztg. 1996, 338: 430 -
4f
Beckert R.Gruner M. Z. Naturforsch., B: Chem. Sci. 1997, 52: 1245 -
4g
Billert T.Beckert R.Fehling P.Döring M.Görls H. Tetrahedron 1997, 53: 5455 -
4h
Käpplinger C.Beckert R.Imhof W. J. Prakt. Chem./Chem.-Ztg. 1998, 340: 323 -
4i
Welzel T.Beckert R.Fischer R.Rau S.Walther D.Görls H. Tetrahedron 2006, 62: 731 - 5
Beckert R.Gruner M. J. Prakt. Chem./Chem.-Ztg. 1992, 334: 611 -
6a
Bulka E.Ahlers KD. Z. Chem. 1963, 3: 348 -
6b
Rossberg H.Pfeiffer WD.Bulka E. Wiss. Z. Ernst-Moritz-Arndt-Univ. Greifsw., Math.-Naturwiss. Reihe 1985, 34: 75 -
6c
Pfeiffer WD.Bulka E.Miethchen R. Z. Chem. 1987, 27: 296 -
6d
Pfeiffer WD.Bulka E. Chem.-Ztg. 1991, 115: 361 -
6e
Pfeiffer WD.Rossberg H. Pharmazie 1993, 48: 732 -
6f
Jira T.Pfeiffer WD.Lachmann K.Epperlein U. Pharmazie 1994, 49: 401 -
6g
Jira T.Stelzer A.Pfeiffer WD.Schopplich Ch.Siegert S.Kindermann M. Pharmazie 1997, 52: 831 -
6h
Koketsu M.Nada F.Ishihara H. Synthesis 2002, 195 -
6i
Geisler K.Pfeiffer WD.Künzler A.Below H .Bulka E .Langer P . Synthesis 2004, 875 -
6j
Geisler K.Künzler A.Below H.Bulka E.Pfeiffer W D.Langer P . Synthesis 2004, 97 -
6k
Sommen GL.Linden A.Heimgartner H. Helv. Chim. Acta 2006, 89: 1322 -
6l
Koketsu M.Kogami M.Ando H.Ishihara H. Synthesis 2006, 31 - 7
Pufky D.Beckert R.Döring M.Walter O. Heterocycles 2002, 57: 1257 -
8a
Fleischhauer J.Beckert R.Günther W.Görls H. Synthesis 2006, 2885 -
8b
Fleischhauer J.Beckert R.Weston J.Schmidt M.Flammersheim H.-J.Görls H. Synthesis 2006, 514 - 9
Beckert R.Fleischhauer J.Darsen A.Weston J.Schenk S.Batista A.Anders E.Görls H.Döring M.Pufky D.Walter O. Heterocycles 2005, 65: 1311 -
10a
Franklin WJ.Werner RL. Tetrahedron Lett. 1965, 34: 3003 -
10b
Barton DHR.Parekh SI.Tajbakhsh M.Theodorakis EA.Tse C.-L. Tetrahedron 1994, 50: 639 -
10c
Atanassov PK.Linden A.Heimgartner H. Helv. Chim. Acta 2004, 87: 1873 - 11
Koketsu M.Yamamura Y.Ishihara H. Synthesis 2006, 2738 -
12a
Beer RJS.McMonagle D.Siddiqui MSS.Hordvik A.Jynge K. Tetrahedron 1979, 35: 1199 -
12b
Fabius B.Cohen-Addad C.Larsen FK.Lehmann MS.Becker P. J. Am. Chem. Soc. 1989, 111: 5728 - 13
Bleiholder C.Gleiter R.Werz DB.Köppel H. Inorg. Chem. 2007, 46: 2249 - 14
Pfeiffer WD.Buhrow J.Bulka E. Wiss. Z. Ernst-Moritz-Arndt-Univ. Greifsw., Math.-Naturwiss. Reihe 1988, 37: 38 - 15
Schröder J.Henke A.Wenzel H.Brandstetter H.Stammler HG.Stammler A.Pfeiffer WD.Tschesche H. J. Med. Chem. 2001, 44: 3231 - 18
Tao J.Perdew JP.Staroverov VN.Scuseria GE. Phys. Rev. Lett. 2003, 91: 146401 - 19
Weigend F.Ahlrichs R. Phys. Chem. Chem. Phys. 2005, 7: 3297 -
20a
Eichkorn K.Treutler O.Öhm H.Häser M.Ahlrichs R. Chem. Phys. Lett. 1995, 240: 283 -
20b
Eichkorn K.Weigend F.Treutler O.Ahlrichs R. Theor. Chem. Acc. 1997, 97: 119 -
20c
Neese F. J. Comput. Chem. 2003, 24: 1740 - 21
Frisch MJ.Trucks GW.Schlegel HB.Scuseria GE.Robb MA.Cheeseman JR.Montgomery JA.Vreven T.Kudin KN.Burant JC.Millam JM.Iyengar SS.Tomasi J.Barone V.Mennucci B.Cossi M.Scalmani G.Rega N.Petersson GA.Nakatsuji H.Hada M.Ehara M.Toyota K.Fukuda R.Hasegawa J.Ishida M.Nakajima T.Honda Y.Kitao O.Nakai H.Klene M.Li X.Knox JE.Hratchian HP.Cross JB.Bakken V.Adamo C.Jaramillo J.Gomperts R.Stratmann RE.Yazyev O.Austin AJ.Cammi R.Pomelli C.Ochterski JW.Ayala PY.Morokuma K.Voth GA.Salvador P.Dannenberg JJ.Zakrzewski VG.Dapprich S.Daniels AD.Strain MC.Farkas O.Malick DK.Rabuck AD.Raghavachari K.Foresman JB.Ortiz JV.Cui Q.Baboul AG.Clifford S.Cioslowski J.Stefanov BB.Liu G.Liashenko A.Piskorz P.Komaromi I.Martin RL.Fox DJ.Keith T.Al-Laham MA.Peng CY.Nanayakkara A.Challacombe M.Gill PMW.Johnson B.Chen W.Wong MW.Gonzalez C.Pople JA. Gaussian03, revision D.01 Gaussian Inc.; Wallingford CT: 2004. see: http://www.gaussian.com -
22a
Becke AD. Phys. Rev. A: At., Mol., Opt. Phys. 1988, 38: 3098 -
22b
Becke AD. J. Chem. Phys. 1993, 98: 5648 -
22c
Lee C.Yang W.Parr RG. Phys. Rev. B: Condens. Matter Mater. Phys. 1988, 37: 785 -
23a
Hehre WJ.Ditchfield R.Pople JA. J. Chem. Phys. 1972, 56: 2257 -
23b
Hariharan PC.Pople JA. Theor. Chim. Acta 1973, 28: 213 -
23c
Francl MM.Pietro WJ.Hehre WJ.Binkley JS.Gordon MS.DeFrees DJ.Pople JA. J. Chem. Phys. 1982, 77: 3654 - 25
COLLECT, Data Collection Software
Nonius B.V.;
Delft/The Netherlands:
1998.
- 26
Otwinowski Z.Minor W. Processing of X-Ray Diffraction Data Collected in Oscillation Mode, In Methods in Enzymology Vol. 276 Macromolecular Crystallography:Carter CW.Sweet RM. Academic Press; New York: 1997. Part A. p.307-326 - 27
Sheldrick GM. Acta Crystallogr., Sect. A 1990, 46: 467 - 28
Sheldrick GM. SHELXL-97 (Release 97-2) University of Göttingen; Germany: 1997. - 29
XP. Version 4.1
Siemens Analytical X-ray Instruments Inc.;
Madison/Wisconsin:
1990.
References
Orca - an ab initio, DFT, and semiempirical scf-mo package; see: http://www.thch.uni-bonn.de/tc/orca.
17Weinhold, F. NBO, version 5; see:
http://www.chem.wisc.edu/˜nbo5/.
CCDC-644462 (3), CCDC-644463 (7g), and CCDC-644464 (8j) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge via www.ccdc.cam.ac.uk/conts/retrieving.html (or from the Cambridge Crystallographic Data Centre, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44(1223)336033; email: deposit@ccdc.cam.ac.uk).