메뉴 건너뛰기




Volumn 38, Issue 12, 2008, Pages 2043-2053

Solvent-free synthesis of 2-amino-3-aryl-5-substituted thiophenes as anti-inflammatory agents using KF-Al2O3 under microwave irradiation

Author keywords

2 Amino 3 aryl 5 substituted thiophenes; Anti inflammatory agents; KF Al 2O3; Microwave irradiation

Indexed keywords

(4 BROMO PHENYL) (5 MORPHOLIN 4 YL 4 PHENYL THIOPENE 2 YL) METHANONE; 4 (1 BENZYLSULFANYL 2 PHENYL BUTA 1,3 DIENYL) MORPHOLINE; 4 BIPHENYL 4 YL 5 MORPHOLIN 4 YL THIOPENE 2 CARBOXYLIC ACID ETHYL ESTER; 5 MORPHOLIN 4 YL 4 PHENYL THIOPENE 2 CARBOXYLIC ACID (4 CHLORO PHENYL)AMIDE; 5 MORPHOLIN 4 YL 4 PHENYL THIOPENE 2 CARBOXYLIC ACID 3 TOLYLAMIDE; 5 MORPHOLIN 4 YL 4 PHENYL THIOPENE 2 CARBOXYLIC ACID NAPHTHALENE 1 YLAMIDE; ANTIINFLAMMATORY AGENT; THIOPENE DERIVATIVE;

EID: 45749119977     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910801997843     Document Type: Article
Times cited : (17)

References (25)
  • 2
    • 33846029182 scopus 로고    scopus 로고
    • Habibi, D.; Marvi, O. Montmorillonite KSF clay as an efficient catalyst for the synthesis of 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides under solvent-free conditions using microwave irradiation. Catal. Commun. 2007, 8, 127.
    • Habibi, D.; Marvi, O. Montmorillonite KSF clay as an efficient catalyst for the synthesis of 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides under solvent-free conditions using microwave irradiation. Catal. Commun. 2007, 8, 127.
  • 3
    • 0009860642 scopus 로고    scopus 로고
    • Fast synthesis of aryl triflates with controlled microwave heating
    • Bengtson, A.; Hallberg, A.; Larhed, M. Fast synthesis of aryl triflates with controlled microwave heating. Org. Lett. 2002, 4, 1231.
    • (2002) Org. Lett , vol.4 , pp. 1231
    • Bengtson, A.1    Hallberg, A.2    Larhed, M.3
  • 4
    • 1142276334 scopus 로고    scopus 로고
    • Efficient palladium/copper cocatalyzed C-N coupling reaction of unactivated aryl bromide or iodide with amino acid under microwave heating
    • Xu, L. W.; Xia, C. G.; Li, J. W.; Li, F. W.; Zhou, S. L. Efficient palladium/copper cocatalyzed C-N coupling reaction of unactivated aryl bromide or iodide with amino acid under microwave heating. Catal. Commun. 2004, 5, 121.
    • (2004) Catal. Commun , vol.5 , pp. 121
    • Xu, L.W.1    Xia, C.G.2    Li, J.W.3    Li, F.W.4    Zhou, S.L.5
  • 5
    • 33645969594 scopus 로고    scopus 로고
    • Fast and selective synthesis of novel cyclic sulfamide HIV-1 protease inhibitors under controlled microwave heating
    • Gold, H.; Ax, A.; Vrang, L.; Samuelsson, B.; Karlen, A.; Hallberg, A.; Larhed, K. M.; Anders, H.; Mats, L. Fast and selective synthesis of novel cyclic sulfamide HIV-1 protease inhibitors under controlled microwave heating. Tetrahedron 2006, 62, 4671.
    • (2006) Tetrahedron , vol.62 , pp. 4671
    • Gold, H.1    Ax, A.2    Vrang, L.3    Samuelsson, B.4    Karlen, A.5    Hallberg, A.6    Larhed, K.M.7    Anders, H.8    Mats, L.9
  • 6
    • 33646098177 scopus 로고    scopus 로고
    • Novelties of low energy microwave irradiation in tri-phase vis-à-vis bi-liquid phase-transfer catalysis in selective etherification of aromatic phenols
    • Yadav, G. D.; Desai, N. M. Novelties of low energy microwave irradiation in tri-phase vis-à-vis bi-liquid phase-transfer catalysis in selective etherification of aromatic phenols. Catal. Commun. 2006, 7, 325.
    • (2006) Catal. Commun , vol.7 , pp. 325
    • Yadav, G.D.1    Desai, N.M.2
  • 8
    • 3042517262 scopus 로고    scopus 로고
    • An efficient and facile one-step synthesis of highly substituted thiophenes
    • Moghaddam, M. F.; Zali- Boinee, H. An efficient and facile one-step synthesis of highly substituted thiophenes. Tetrahedron 2004, 60, 6085.
    • (2004) Tetrahedron , vol.60 , pp. 6085
    • Moghaddam, M.F.1    Zali- Boinee, H.2
  • 9
    • 3843137260 scopus 로고    scopus 로고
    • Design synthesis and pharmacological evaluation of some 2-[4-morpholino]-5-substituted thiophenes as novel anti-inflammtory agents; generation of a novel anti-inflammatory pharmacophore
    • Pillai, A. D.; Rathod, P. D.; Xavier, F. P.; Vasu, K. K.; Padh, H.; Sudarsanam, V. Design synthesis and pharmacological evaluation of some 2-[4-morpholino]-5-substituted thiophenes as novel anti-inflammtory agents; generation of a novel anti-inflammatory pharmacophore. Bio. Med. Chem. 2004, 12, 4667.
    • (2004) Bio. Med. Chem , vol.12 , pp. 4667
    • Pillai, A.D.1    Rathod, P.D.2    Xavier, F.P.3    Vasu, K.K.4    Padh, H.5    Sudarsanam, V.6
  • 10
  • 11
    • 0012770630 scopus 로고
    • A new Porphyrin synthesis. The synthesis of Porphin
    • Rothemunt, P. A new Porphyrin synthesis. The synthesis of Porphin. J. Am. Chem. Soc. 1936, 58, 625.
    • (1936) J. Am. Chem. Soc , vol.58 , pp. 625
    • Rothemunt, P.1
  • 12
    • 0037060932 scopus 로고    scopus 로고
    • Synthesis and characterisation of N,N-disubstituted 2-amino-5-acylthiophenes and 2-amino-5-acylthiazoles
    • Noack, A.; Hartman, H. Synthesis and characterisation of N,N-disubstituted 2-amino-5-acylthiophenes and 2-amino-5-acylthiazoles. Tetrahedron 2002, 58, 2137.
    • (2002) Tetrahedron , vol.58 , pp. 2137
    • Noack, A.1    Hartman, H.2
  • 13
    • 84860875380 scopus 로고
    • Heterocyclen aus CH-aciden Nitrilen, VIII. 2-Amino-thiophene aus methylenaktiven Nitrilen, Carbonylverbindungen und Schewefel
    • Gewald, K.; Schinke, E.; Bottcher, H. Heterocyclen aus CH-aciden Nitrilen, VIII. 2-Amino-thiophene aus methylenaktiven Nitrilen, Carbonylverbindungen und Schewefel. Chem. Ber. 1966, 99, 94.
    • (1966) Chem. Ber , vol.99 , pp. 94
    • Gewald, K.1    Schinke, E.2    Bottcher, H.3
  • 14
    • 0034603585 scopus 로고    scopus 로고
    • The synthesis of 5-alkoxy and 5-amino substituted thiophenes
    • Pinto, I. L.; Jarvest, R. L.; Serafinowska, H. T. The synthesis of 5-alkoxy and 5-amino substituted thiophenes. Tetrahedron Lett. 2000, 41, 1597.
    • (2000) Tetrahedron Lett , vol.41 , pp. 1597
    • Pinto, I.L.1    Jarvest, R.L.2    Serafinowska, H.T.3
  • 15
    • 0033778397 scopus 로고    scopus 로고
    • A simple route to N,N-dialkyl derivatives of 2-amino-5-thiophenecarboxylates
    • Heyde, C.; Zug, I.; Hartmann, H. A simple route to N,N-dialkyl derivatives of 2-amino-5-thiophenecarboxylates. Eur. J. Org. Chem. 2000, 3273.
    • (2000) Eur. J. Org. Chem , pp. 3273
    • Heyde, C.1    Zug, I.2    Hartmann, H.3
  • 16
    • 34247630662 scopus 로고    scopus 로고
    • Controlled microwave-assisted synthesis of ZnO nanopowder and its catalytic activity for O-acylation of alcohol and phenol
    • Moghaddam, M. F.; Saeidian, H. Controlled microwave-assisted synthesis of ZnO nanopowder and its catalytic activity for O-acylation of alcohol and phenol. Mater. Sci. Eng. B. 2007, 139, 265.
    • (2007) Mater. Sci. Eng. B , vol.139 , pp. 265
    • Moghaddam, M.F.1    Saeidian, H.2
  • 17
    • 36248977640 scopus 로고    scopus 로고
    • ZnO nanoparticles: An efficient nanocatalyst for the synthesis of β-acetamido ketones/esters via a multi-component reaction
    • Mirjafary, Z.; Saeidian, H.; Sadeghi, A.; Moghaddam, M. F. ZnO nanoparticles: An efficient nanocatalyst for the synthesis of β-acetamido ketones/esters via a multi-component reaction. Catal. Commun. 2008, 9, 299.
    • (2008) Catal. Commun , vol.9 , pp. 299
    • Mirjafary, Z.1    Saeidian, H.2    Sadeghi, A.3    Moghaddam, M.F.4
  • 18
    • 21544464331 scopus 로고    scopus 로고
    • Oxidative cyclization of thiobenzanilides to benzothiazoles using N-benzyl-DABCO tribromide under mild conditions
    • Moghaddam, M. F.; Zali-Boinee, H. Oxidative cyclization of thiobenzanilides to benzothiazoles using N-benzyl-DABCO tribromide under mild conditions. Synlett 2005, 1612.
    • (2005) Synlett , pp. 1612
    • Moghaddam, M.F.1    Zali-Boinee, H.2
  • 19
    • 0042848826 scopus 로고    scopus 로고
    • A versatile one-pot synthesis of 2,3,5-tri-substituted thiohenes from thiomorpholides
    • Moghaddam, M. F.; Zali-Boinee, H. A versatile one-pot synthesis of 2,3,5-tri-substituted thiohenes from thiomorpholides. Tetrahedron Lett. 2003, 44, 6253.
    • (2003) Tetrahedron Lett , vol.44 , pp. 6253
    • Moghaddam, M.F.1    Zali-Boinee, H.2
  • 20
    • 0034728930 scopus 로고    scopus 로고
    • Thia-Fries rearrangement of aryl sulfonates in dry media under microwave activation
    • Moghaddam, M. F.; Dekamin, M. G. Thia-Fries rearrangement of aryl sulfonates in dry media under microwave activation. Tetrahedron Lett. 2000, 41, 3479.
    • (2000) Tetrahedron Lett , vol.41 , pp. 3479
    • Moghaddam, M.F.1    Dekamin, M.G.2
  • 21
    • 33846697730 scopus 로고    scopus 로고
    • Facile Double fries rearrangement of diesters under microwave irradiation; application to the synthesis of a biogenetically rare type of natural phenol
    • Moghaddam, M. F.; Porkaleh, H.; Zali-Boinee, H. Facile Double fries rearrangement of diesters under microwave irradiation; application to the synthesis of a biogenetically rare type of natural phenol. Lett. Org. Chem. 2006, 3, 123.
    • (2006) Lett. Org. Chem , vol.3 , pp. 123
    • Moghaddam, M.F.1    Porkaleh, H.2    Zali-Boinee, H.3
  • 22
    • 0035098092 scopus 로고    scopus 로고
    • Microwave- assisted rapid hydrolysis and preparation of thioamides by Wilgerodt-Kindler reaction
    • Moghaddam, M. F.; Ghafarzadeh, H. Microwave- assisted rapid hydrolysis and preparation of thioamides by Wilgerodt-Kindler reaction. Synth. Commun. 2001, 31, 317.
    • (2001) Synth. Commun , vol.31 , pp. 317
    • Moghaddam, M.F.1    Ghafarzadeh, H.2
  • 23
    • 38049123786 scopus 로고    scopus 로고
    • KF-Al203 promoted synthesis of fully substituted new indeno- and naphtho-fused thiophenes under solvent-free conditions by controlled microwave heating
    • Moghaddam, M. F.; Saeidian, H.; Mirjafary, Z.; Sadeghi, A. KF-Al203 promoted synthesis of fully substituted new indeno- and naphtho-fused thiophenes under solvent-free conditions by controlled microwave heating. Lett. Org. Chem. 2007, 4, 576.
    • (2007) Lett. Org. Chem , vol.4 , pp. 576
    • Moghaddam, M.F.1    Saeidian, H.2    Mirjafary, Z.3    Sadeghi, A.4
  • 25
    • 0025983750 scopus 로고
    • Selective desilylation of tert-butyldimethylsilyl ethers of phenols using potassium fluoride-alumina and ultrasound
    • Schmittiling, A. E.; Sawyer, J. S. Selective desilylation of tert-butyldimethylsilyl ethers of phenols using potassium fluoride-alumina and ultrasound. Tetrahedron Lett. 1991, 32, 7207.
    • (1991) Tetrahedron Lett , vol.32 , pp. 7207
    • Schmittiling, A.E.1    Sawyer, J.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.