HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine → N-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine | HCID 17743497 | — |
| Reactant | HCID 178524800 | HCID 178524800 | — |
| Product | N-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamide | HCID 178521857 | — |
Reaction Steps
N-(6-Chloro-2,3,4,9-tetrahydro-1H-carbazol-1-yl)-1H-imidazole-4-carboxamide was prepared from 4-imidazole carboxylic acid and 6-chloro-2,3,4,9-tetrahydro-1H-carbazol-1-amine in a similar manner as described above to give a white solid (4% yield). 1H-NMR (CDCl3): δ 9.19 (s, 1H), 7.62 (s, 1H), 7.57 (s, 1H), 7.41 (s, 1H), 7.37 (d, 1H), 7.17 (d, 1H), 7.05 (dd, 1H), 6.60 (d, 1H), 5.25 (m, 1H), 2.62 (m, 2H), 2.21 (m, 1H), 1.91 (m, 3H); MS m/z 313 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07419997B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-98fa6796a8f14b7fa694ff5979cb375b |
| Source note | uspto-grants-2008_09 |