Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement
3-Arylaminoisoxazol-5(2H)-ones, substituted on nitrogen with benzoxazole and benzothiazole groups react with triethylamine in ethanol under reflux to afford the corresponding indole and imidazobenzothiazole derivatives, respectively.
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| Format: | Article |
| Language: | English |
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Sociedade Brasileira de Química
2006-01-01
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| Series: | Journal of the Brazilian Chemical Society |
| Subjects: | |
| Online Access: | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000300021 |
| _version_ | 1818980191637078016 |
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| author | Khalafy Jabbar Marjani Ahmad Poursattar Ebrahimlo Ali Reza Molla |
| author_facet | Khalafy Jabbar Marjani Ahmad Poursattar Ebrahimlo Ali Reza Molla |
| author_sort | Khalafy Jabbar |
| collection | DOAJ |
| description | 3-Arylaminoisoxazol-5(2H)-ones, substituted on nitrogen with benzoxazole and benzothiazole groups react with triethylamine in ethanol under reflux to afford the corresponding indole and imidazobenzothiazole derivatives, respectively. |
| first_indexed | 2024-12-20T17:11:30Z |
| format | Article |
| id | doaj.art-53ab0547bdc642418f85e6e0b388e7a5 |
| institution | Directory Open Access Journal |
| issn | 0103-5053 1678-4790 |
| language | English |
| last_indexed | 2024-12-20T17:11:30Z |
| publishDate | 2006-01-01 |
| publisher | Sociedade Brasileira de Química |
| record_format | Article |
| series | Journal of the Brazilian Chemical Society |
| spelling | doaj.art-53ab0547bdc642418f85e6e0b388e7a52022-12-21T19:32:07ZengSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society0103-50531678-47902006-01-01173570576Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangementKhalafy JabbarMarjani Ahmad PoursattarEbrahimlo Ali Reza Molla3-Arylaminoisoxazol-5(2H)-ones, substituted on nitrogen with benzoxazole and benzothiazole groups react with triethylamine in ethanol under reflux to afford the corresponding indole and imidazobenzothiazole derivatives, respectively.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000300021isoxazolones2-chlorobenzoxazole2-chlorobenzothiazoleindolesimidazobenzothiazolestriethylaminebase induced rearrangements |
| spellingShingle | Khalafy Jabbar Marjani Ahmad Poursattar Ebrahimlo Ali Reza Molla Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement Journal of the Brazilian Chemical Society isoxazolones 2-chlorobenzoxazole 2-chlorobenzothiazole indoles imidazobenzothiazoles triethylamine base induced rearrangements |
| title | Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement |
| title_full | Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement |
| title_fullStr | Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement |
| title_full_unstemmed | Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement |
| title_short | Synthesis of new N-Benzoxazole and N-Benzothiazole derivatives of 3-(4-Substituted- phenyl)aminoisoxazol-5(2H)-ones and comparison of their base induced rearrangement |
| title_sort | synthesis of new n benzoxazole and n benzothiazole derivatives of 3 4 substituted phenyl aminoisoxazol 5 2h ones and comparison of their base induced rearrangement |
| topic | isoxazolones 2-chlorobenzoxazole 2-chlorobenzothiazole indoles imidazobenzothiazoles triethylamine base induced rearrangements |
| url | http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532006000300021 |
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