Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate
The title compound (2) was prepared in high yield by catalytic transfer hydrogenation of the 6-nitro precursor (1), using hydrazine hydrate as the hydrogen source. Under the conditions employed, the ester groups remain unaffected. The new compound was fully characterised by elemental analysis, 1H-NM...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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MDPI AG
2015-03-01
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| Series: | Molbank |
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| Online Access: | http://www.mdpi.com/1422-8599/2015/1/M849 |
| _version_ | 1818033579090771968 |
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| author | Norbert Haider Katharina Tropper |
| author_facet | Norbert Haider Katharina Tropper |
| author_sort | Norbert Haider |
| collection | DOAJ |
| description | The title compound (2) was prepared in high yield by catalytic transfer hydrogenation of the 6-nitro precursor (1), using hydrazine hydrate as the hydrogen source. Under the conditions employed, the ester groups remain unaffected. The new compound was fully characterised by elemental analysis, 1H-NMR, 13C-NMR, MS and HRMS data. |
| first_indexed | 2024-12-10T06:25:30Z |
| format | Article |
| id | doaj.art-40e11299a2d94a0cb58688eb764b8330 |
| institution | Directory Open Access Journal |
| issn | 1422-8599 |
| language | English |
| last_indexed | 2024-12-10T06:25:30Z |
| publishDate | 2015-03-01 |
| publisher | MDPI AG |
| record_format | Article |
| series | Molbank |
| spelling | doaj.art-40e11299a2d94a0cb58688eb764b83302022-12-22T01:59:14ZengMDPI AGMolbank1422-85992015-03-0120151M84910.3390/M849M849Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylateNorbert Haider0Katharina Tropper1Department of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, Althanstraße 14, A-1090 Vienna, AustriaDepartment of Pharmaceutical Chemistry, Faculty of Life Sciences, University of Vienna, Althanstraße 14, A-1090 Vienna, AustriaThe title compound (2) was prepared in high yield by catalytic transfer hydrogenation of the 6-nitro precursor (1), using hydrazine hydrate as the hydrogen source. Under the conditions employed, the ester groups remain unaffected. The new compound was fully characterised by elemental analysis, 1H-NMR, 13C-NMR, MS and HRMS data.http://www.mdpi.com/1422-8599/2015/1/M849catalytic transfer hydrogenationhydrazine hydrateaminocarbazoles |
| spellingShingle | Norbert Haider Katharina Tropper Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate Molbank catalytic transfer hydrogenation hydrazine hydrate aminocarbazoles |
| title | Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate |
| title_full | Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate |
| title_fullStr | Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate |
| title_full_unstemmed | Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate |
| title_short | Dimethyl 6-Amino-1-methyl-9H-carbazole-2,3-dicarboxylate |
| title_sort | dimethyl 6 amino 1 methyl 9h carbazole 2 3 dicarboxylate |
| topic | catalytic transfer hydrogenation hydrazine hydrate aminocarbazoles |
| url | http://www.mdpi.com/1422-8599/2015/1/M849 |
| work_keys_str_mv | AT norberthaider dimethyl6amino1methyl9hcarbazole23dicarboxylate AT katharinatropper dimethyl6amino1methyl9hcarbazole23dicarboxylate |