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One-pot synthesis of 1,3-thiazolidin-4-one using Bi(SCH_2COOH)_3 as catalyst 被引量:2

One-pot synthesis of 1,3-thiazolidin-4-one using Bi(SCH_2COOH)_3 as catalyst
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摘要 A catalytic multi-component reaction involving aromatic amine,aromatic aldehydes,mercapto acid as substrates and Bi(SCH_2COOH)_3 as catalyst under solvent free conditions,afforded thiazolidin-4-one in good yields.The efficiency of the catalyst was proved with a variety of substrates,ranging from electrondeficient to electron-rich aldehydes. A catalytic multi-component reaction involving aromatic amine,aromatic aldehydes,mercapto acid as substrates and Bi(SCH_2COOH)_3 as catalyst under solvent free conditions,afforded thiazolidin-4-one in good yields.The efficiency of the catalyst was proved with a variety of substrates,ranging from electrondeficient to electron-rich aldehydes.
出处 《Chinese Chemical Letters》 SCIE CAS CSCD 2013年第5期389-391,共3页 中国化学快报(英文版)
基金 North Tehran Branch,Islamic Azad University for their financial support
关键词 Thiazolidin-4-one Mercapto acid Multicomponent Thioglycolic acid Thiazolidin-4-one Mercapto acid Multicomponent Thioglycolic acid
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  • 1王忠义,史海健,郑和根,史好新,郑爱华,杨周生,马越鸣,董群.2-硫代-4-噻唑啉酮衍生物的合成[J].有机化学,1994,14(2):190-194. 被引量:5
  • 2DANDIA, Anshu SINGH, Ruby SARAWGI, Pritima KHATURIA, Sarita.Multicomponent One-pot Diastereoselective Synthesis of Biologically Important Scaffold under Microwaves[J].Chinese Journal of Chemistry,2006,24(7):950-954. 被引量:9
  • 3K.Takasu,H.Inoue,H.S.Kim,et al.J.Med.Chem.45(2002) 995.
  • 4J.S.Modica-Napolitano,K.Koya,E.Weisberg,et al.Cancer Res.56(1996) 544.
  • 5R.Wadhwa,T.Sugihara,A.Yoshida,et al.Cancer Res.60(2000) 6818.
  • 6J.Li,Y.Chen,J.Sperry,et al.Med.Chem.Commun.2(2011) 229.
  • 7I.Naasani,H.Seimiya,T.Yamori,et al.Cancer Res.59(1999) 4004.
  • 8C.E.Redemann,R.N.Icke,G.A.Alles,et al.Org.Synth.3(1955) 763.
  • 9Data for new compounds.5a:yield 25.4%.mp:301-303℃;ESI-MS:m/z 355.2[M] ~+,126.9[M] ~-;~1H NMR(300 MHz,DMSO-d_6):δ3.38(s, 3H),3.77(s,3H),7.36-7.27(m,1H),7.47(m,1H),7.56(d,1H,J = 8.2 Hz),7.88(d,1H,J = 7.3 Hz),8.29(m,2H),8.73-8.59(m,1H),9.12(m, 2H).5b:yield 36.5%.mp 294-296℃;ESI-MS:m/z 383.3[M] ~+,126.9[M] ~-;~1H NMR(300 MHz,DMSO-d_6):δ1.33(t,3H),2.68(s,3H),3.77 (s,3H),3.97(q,2H),7.32(dd,1H),7.48(dd,1H),7.56(d,1H,J = 8.2 Hz),7.88(d,1H,J = 7.6 Hz),8.12(d,2H,J = 6.5 Hz),9.01(d,2H, J = 6.7 Hz).5c:yield 31.7%.mp 277-279℃;ESI-MS:m/z 395.4[M] ~+,126.9[M] ~-;~1H NMR(300 MHz,DMSO-d_6):δ1.24-1.04(m,4H), 2.68(s,3H),2.96-2.84(m,1H),3.74(s,3H),7.28(dd,1H),7.45(dd,1H),7.53(d,1H,J = 8.2 Hz),7.86(d,1H,J = 7.8 Hz),8.12(d,2H, J = 6.6 Hz),8.97(d,2H,J = 6.6 Hz).5d:yield 28.9%.mp 290-293℃;ESI-MS:m/z 403.3[M] ~+,126.9[M] ~+;~1H NMR(300 MHz,DMSO-d_6):δ2.68(s,3H),3.73(s,3H),3.37(s,3H),7.58-7.45(m,2H),8.03(s,1H),8.13(d,2H,J = 6.4 Hz),8.95(d,2H,J = 6.5 Hz).5e:yield 32.8%.mp 274-276℃;ESI-MS:m/z417.4[M] ~+,126.9[M] ~-;~1H NMR(300 MHz,DMSO-.
  • 10Kavitha,C.V.; Doreswamy,S.; Sridhar,M.A.; Prasadb,J.S.; Kanchugarakoppal,S.R.Bioorg.Med.Chem.2006,14,2290.

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