HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine → HCID 11452625, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine | HCID 597879 | — |
| Reactant | 2-Chloro-5-(trifluoromethyl)pyrimidine | HCID 13317019 | — |
| Product | HCID 11452625 | HCID 11452625 | — |
Reaction Steps
6-Bromo-N-[5-(trifluoromethyl)pyrimidin-2-yl]-2,3,4,9-tetrahydro-1H-carbazol-1-amine was prepared from 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine (75 mg, 0.28 mmol) and 2-chloro-5-(trifluoromethyl)-pyrimidine (0.5 mL) in a similar manner as described in Example 22 to give 5 mg (4%) of a yellow solid. 1H-NMR (DMSO-d6) taken at 80° C.: δ 10.94-10.88 (m, 1H), 8.69-8.62 (m, 1H), 8.30-8.24 (m, 1H), 7.55 (s, 1H), 7.21 (d, 1H), 7.13-7.10 (m, 1H), 7.02 (d, 1H), 5.40-5.27 (m, 1H), 2.62-2.58 (m, 2H), 2.08-1.96 (m, 2H), 1.87-1.76 (m, 2H); MS m/z (M−1) 409, 411.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351733B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-9594617a2f7a4f7da87656c37c79faa6 |
| Source note | uspto-grants-2008_04 |