Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest

The title compounds (4a,b) were prepared by chloroacetylation of 2-acyl-3-aminobenzofuran(1a,b) and subsequent treatment with hexamethylene tetramine in ethanol via the complex salts (3a,b). Similar reaction with ethyl 3-aminobenzofuran-2 carboxylate (5) produced 3H-benzofuro[3,2-e]-1,4-diazepin2,5(...

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Main Authors: K. M. Basavaraja, V. P. Vaidya, C. Chandrashekhar
Format: Article
Language:English
Published: Wiley 2008-01-01
Series:E-Journal of Chemistry
Online Access:http://dx.doi.org/10.1155/2008/920926
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author K. M. Basavaraja
V. P. Vaidya
C. Chandrashekhar
author_facet K. M. Basavaraja
V. P. Vaidya
C. Chandrashekhar
author_sort K. M. Basavaraja
collection DOAJ
description The title compounds (4a,b) were prepared by chloroacetylation of 2-acyl-3-aminobenzofuran(1a,b) and subsequent treatment with hexamethylene tetramine in ethanol via the complex salts (3a,b). Similar reaction with ethyl 3-aminobenzofuran-2 carboxylate (5) produced 3H-benzofuro[3,2-e]-1,4-diazepin2,5(1H,4H)-dione (7) in good yield. All the newly synthesized compounds are characterized by elemental analysis and spectral studies, and evaluated for antimicrobial and anticonvulsant activities.
format Article
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institution Kabale University
issn 0973-4945
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language English
publishDate 2008-01-01
publisher Wiley
record_format Article
series E-Journal of Chemistry
spelling doaj-art-2b40f5c00d894f07b67132f1329dd6102025-02-03T06:11:22ZengWileyE-Journal of Chemistry0973-49452090-98102008-01-015356757110.1155/2008/920926Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological InterestK. M. Basavaraja0V. P. Vaidya1C. Chandrashekhar2Department of Industrial Chemistry, Gulberga University, Jnana Ganga, Bellary-Dist: Bellary, Karnataka, IndiaDepartment of Chemistry, Kuvempu University, Jnana Sahyadri, Shankaraghatta-577451 Dist: Shimoga, Karnataka, IndiaDepartment of Chemistry, Kuvempu University, Jnana Sahyadri, Shankaraghatta-577451 Dist: Shimoga, Karnataka, IndiaThe title compounds (4a,b) were prepared by chloroacetylation of 2-acyl-3-aminobenzofuran(1a,b) and subsequent treatment with hexamethylene tetramine in ethanol via the complex salts (3a,b). Similar reaction with ethyl 3-aminobenzofuran-2 carboxylate (5) produced 3H-benzofuro[3,2-e]-1,4-diazepin2,5(1H,4H)-dione (7) in good yield. All the newly synthesized compounds are characterized by elemental analysis and spectral studies, and evaluated for antimicrobial and anticonvulsant activities.http://dx.doi.org/10.1155/2008/920926
spellingShingle K. M. Basavaraja
V. P. Vaidya
C. Chandrashekhar
Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
E-Journal of Chemistry
title Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
title_full Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
title_fullStr Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
title_full_unstemmed Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
title_short Synthesis of Benzofuro[3,2-e]-1,4-diazepines of Pharmacological Interest
title_sort synthesis of benzofuro 3 2 e 1 4 diazepines of pharmacological interest
url http://dx.doi.org/10.1155/2008/920926
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