Subscribe to RSS
DOI: 10.1055/s-2008-1032180
Efficient Syntheses of Some Versatile 3,5-Bifunctional Pyrazole Building Blocks
Publication History
Publication Date:
18 February 2008 (online)
Abstract
A series of convenient synthetic procedures are reported for pyrazole derivatives with carbonyl or ester groups in the 3- and 5-positions and variable substitution pattern at C4 and at the functional side arms. All compounds have been characterized by 1H and 13C NMR spectroscopy, elemental analyses, and mass spectrometry. In addition, the structures of several pyrazole derivatives have been determined by single crystal X-ray diffraction, which provides insight into the effect of functional side arms on the hydrogen-bonded supramolecular motifs of NH-pyrazoles.
Key words
pyrazoles - N-heterocycles - X-ray crystal structure - H-bonding
- 1
Dvorak CA.Rudolph DA.Ma S.Carruthers NI. J. Org. Chem. 2005, 70: 4188 -
2a
Trofimenko S. Prog. Inorg. Chem. 1986, 34: 115 -
2b
La Monica G.Ardizzoia GA. Prog. Inorg. Chem. 1997, 46: 151 - 4
Rzepecki P.Geib N.Pfeifer M.Biesemeier F.Schrader T. J. Org. Chem. 2007, 72: 3614 - 5
Noël G.Röder JC.Dechert S.Pritzkow H.Bolk L.Mecking S.Meyer F. Adv. Synth. Catal. 2006, 348: 887 -
6a
Aggarwal VK.de Vicente J.Bonnert RV. J. Org. Chem. 2003, 68: 5381 -
6b
Bishop BC.Brands KMJ.Gibb AD.Kennedy DJ. Synthesis 2004, 43 -
6c
Padwa A. 1,3-Dipolar Cycloaddition Chemistry Vol 1: Wiley; New York: 1984. -
6d
Stanovnik B.Svete J. In Science of Synthesis Vol. 12:Neier R. Thieme; Stuttgart: 2002. p.15-225 - 7
Röder JC.Meyer F.Konrad M.Sandhöfner S.Kaifer E.Pritzkow H. Eur. J. Org. Chem. 2001, 4479 - 8
Cacchi S.Fabrizi G.Carangio A. Synlett 1997, 959 - 9
Arán VJ.Kumar M.Molina J.Lamarque L.Navarro P.Garcia-España E.Ramirez JA.Luis SV.Escuder B. J. Org. Chem. 1999, 64: 6135 - 10
Acerete C.Bueno JM.Campayo L.Navarro P.Rodríguez-Franco MI.Samat A. Tetrahedron 1994, 50: 4765 - 11
Schenck T.Milne C.Sawyer J.Bosnich B. Inorg. Chem. 1985, 24: 2334 - 12
Foces-Foces C.Alkorta I.Elguero J. Acta Crystallogr., Sect. B 2000, 56: 1018 - 13
Jung ME.Min S.-J.Houk KN.Ess D. J. Org. Chem. 2004, 69: 9085 - 14
Rodríguez-Franco MI.Dorronsoro I.Hernández-Higueras AI.Antequera G. Tetrahedron Lett. 2001, 42: 863 - 15
Wolff L. Justus Liebigs Ann. Chem. 1902, 325: 186 - 16
Buchner E.v. Heide C. Ber. Dtsch. Chem. Ges. 1902, 35: - 17
Claramunt RM.Cornago P.Torres V.Pinilla E.Torres MR.Samat A.Lokshin V.Valés M.Elguero J. J. Org. Chem. 2006, 71: 6881 - 18
Minkin VI.Garnovskii AD. Adv. Heterocycl. Chem. 2000, 76: 157 - 19
Fayos J.Infantes L.Cano FH. Cryst. Growth Des. 2005, 1: 191 - 20
Infantes L.Motherwell S. Struct. Chem. 2004, 3: 173 - 21
Myhre PC.Maxey CT.Bebout DC.Swedberg SH.Petersen BL. J. Org. Chem. 1990, 55: 3417 - 22
Meth-Cohn O.Vuorinen E.Modro TA. J. Org. Chem. 1989, 54: 4822 -
23a
Sheldrick GM. SHELXL-97, Program for Crystal Structure Refinement University of Göttingen; Göttingen: 1997. -
23b
Sheldrick GM. SHELXS-97, Program for Crystal Structure Solution University of Göttingen; Göttingen: 1997. -
23c
X-AREA
STOE & CIE GmbH;
Darmstadt:
2002.
-
23d
X-RED
STOE & CIE GmbH;
Darmstadt:
2002.
References
Klingele, J.; Dechert, S.; Meyer, F. Coord. Chem. Rev., manuscript in preparation.
24CCDC-664760 (2), CCDC-664761 (5), CCDC-664762 (6), and CCDC-664763 (8) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge at 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; E-mail: deposit@ccdc.cam.ac.uk].