RSS-Feed abonnieren
DOI: 10.1055/s-2003-44357
A Concise Synthetic Method for Sydnonyl-Substituted Pyrazoline Derivatives
Publikationsverlauf
Publikationsdatum:
03. Dezember 2003 (online)
Abstract
The pyrazolines have been found to have diverse applications in medicine. They are known to be potent antibiotic or antioxidizing agents. Two types of sydnonyl-substituted α,β-unsaturated ketones were synthesized by the Claisen-Schmidt condensation for the preparation of sydnonyl-substituted pyrazolines. One is the condensation of 3-(4-ethoxyphenyl)-4-formylsydnone (1) with acetone (2a) or acetophenone (2b), and the other is the condensation of 4-acetyl-3-arylsydnones 5 with various aryl aldehydes 6. Finally, 1H-pyrazoline derivatives 8 were synthesized successfully by reacting the appropriate α,β-unsaturated ketone precursors 7 with hydrazine hydrate.
Key words
sydnones - 4-acetyl-3-arylsydnones - sydnonyl-substituted α,β-unsaturated ketones - pyrazoles - sydnonyl-substituted pyrazolines
- 1
Sachchar SP.Singh AK. J. Indian Chem. Soc. 1985, 142 - 2
Dambal DB.Pattanashetti PP.Tikare RK.Badami BV.Puranik GS. Indian J. Chem., Sect. B 1984, 23: 186 - 3
Cremlyn RJ.Swinbourne FJ.Mookerjee E. Indian J. Chem., Sect. B 1986, 25: 562 - 4
Kulkarni SE.Mane RA.Ingle DB. Indian J. Chem., Sect. B 1986, 25: 452 - 5
Gawande NG.Shingare MS. Indian J. Chem., Sect. B 1987, 26: 351 - 6
Thakare VG.Wadodkar KN. Indian J. Chem., Sect. B 1986, 25: 610 - 7
Srivastava RP. .Bhaduri AP. Indian J. Chem., Sect. B 1987, 26: 418 - 8
Tökés AL.Janzsó G. Synth. Commun. 1989, 19: 3159 - 9
El-Khawass SM.Farghaly AM.Chaaban I.Fahmy SM. J. Chin. Chem. Soc. (Taipei) 1990, 37: 605 ; Chem. Abstr. 1991, 114, 143225 - 10
Gao C.Hay AS. Synth. Commun. 1995, 25: 1877 - 11
Vishnu Vardhan Reddy K.Sampath Rao P.Ashok D. Synth. Commun. 1998, 29: 2365 - 12
Pinto DCGA.Silva AMS.Cavaleiro JAS. Tetrahedron 1999, 55: 10187 - 13
Müller E.Kálai T.Jekö J.Hideg K. Synthesis 2000, 1415 - 14
DeShong P.Soli ED.Slough GA.Sidler DR.Elango V.Rybczynski PJ.Vosejpka LJS.Lessen TA.Le TX.Anderson GB.von Philipsborn W.Vöhler M.Rentsch D.Zerbe O. J. Organomet. Chem. 2000, 593: 49 - 15
Holla BS.Akberali PM.Shivananda MK. FARMACO 2000, 55: 256 - 16
Ali MM.Doshi AG.Raghuwanshi PB. Synth. Commun. 2000, 30: 3241 - 17
Pathak VN.Pathak R.Gupta R.Oza CK. Synth. Commun. 1997, 27: 1811 - 18
Haunert F.Bolli MH.Hinzen B.Ley SV. J. Chem. Soc., Perkin Trans. 1 1998, 2235 - 19
Bauer U.Egner BJ.Nilsson I.Berghult M. Tetrahedron Lett. 2000, 41: 2713 - 20
Satyanarayana K.Rao MNA. J. Pharm. Sci. 1995, 84: 263 - 21
Satyanarayana K.Rao MNA. Eur. J. Med. Chem. 1995, 30: 641 - 22
Kavali JR.Badami BV. Farmaco 2000, 55: 406 - 23
Turnbull K.Sun C.Krein DM. Tetrahedron Lett. 1998, 39: 1509 - 24
Turnbull K.Krein DM. Synthesis 1996, 1183 - 25
Marx JA.Turnbull K. Tetrahedron Lett. 1993, 34: 239 - 26
Gelvin CR.Turnbull K. Helv. Chim. Acta 1992, 75: 1931 - 27
Burson WC.Jones DR.Turnbull K.Preston PN. Synthesis 1991, 745 - 28
Turnbull K.Blackburn TL.Esterline DT. J. Heterocycl. Chem. 1990, 27: 1259 - 29
Shih MH.Yeh MY. J. Chin. Chem. Soc. (Taipei) 1990, 37: 71 ; Chem. Abstr. 1990, 113, 59034 - 30
Shih MH.Yeh MY. J. Chin. Chem. Soc. (Taipei) 1992, 39: 163 ; Chem. Abstr. 1992, 117, 7317 - 31
Shih MH.Her KH.Yeh MY. J. Chin. Chem. Soc. (Taipei) 2001, 48: 1143 ; Chem. Abstr. 2002, 137, 140455 - 32
Shih MH.Lu LH.Yeh MY. J. Chin. Chem. Soc. (Taipei) 2001, 48: 883 ; Chem. Abstr. 2002, 136, 279403 - 33
Shih MH.Lee MJ.Yeh MY. J. Chin. Chem. Soc. (Taipei) 2002, 49: 361 ; Chem. Abstr. 2003, 138, 170146 - 34
Shih MH. Tetrahedron 2002, 58: 10437 - 35
Shih MH.Yeh MY. Tetrahedron 2003, 59: 4103 - 36
Fokas D.Ryan WJ.Casebier DS.Coffen DL. Tetrahedron Lett. 1998, 39: 2235 - 37
Powers DG.Casebier DS.Fokas D.Ryan WJ.Troth JR.Coffen DL. Tetrahedron 1998, 54: 4085 - 38
Yeh MY.Tien HJ.Huang LY.Chen MH. J. Chin. Chem. Soc. (Taipei) 1983, 30: 29 ; Chem. Abstr. 1983, 99, 105178 - 39
Yeh MY.Tien HJ.Nonaka T. J. Org. Chem. 1983, 48: 1382