Synthesis of some new 2,4-disubstituted thiazoles as possible antibacterial and driti-inflammatory agents
A series of arylthioureas (1), aromatic aldehyde thiosemicarbazones (2) and 5-aryl-2-furfuraldehyde thiosemicarbazones (3) were condensed with 2,4-dichloro-5-fluorophenacyl bromide to yield respective arylaminothiazoles, arylidene/5-aryl-2-furfurylidene hydrazinothiazoles (4). The newly synthesized...
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Published in | European journal of medicinal chemistry Vol. 38; no. 3; pp. 313 - 318 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
PARIS CEDEX 15
Elsevier
01.03.2003
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Subjects | |
Online Access | Get full text |
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Summary: | A series of arylthioureas (1), aromatic aldehyde thiosemicarbazones (2) and 5-aryl-2-furfuraldehyde thiosemicarbazones (3) were condensed with 2,4-dichloro-5-fluorophenacyl bromide to yield respective arylaminothiazoles, arylidene/5-aryl-2-furfurylidene hydrazinothiazoles (4). The newly synthesized compounds were characterized by IR, H-1-NMR and mass spectral studies. These compounds were also screened for their antibacterial and anti-inflammatory activities. Two of the newly synthesized compounds showed anti-inflammatory activity comparable with that of Ibuprofen. (C) 2003 Editions scientifiques et medicales Elsevier SAS. All rights reserved. |
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ISSN: | 0223-5234 |
DOI: | 10.1016/S0223-5234(02)01447-2 |