HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine → HCID 11338120, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-bromo-2,3,4,9-tetrahydro-1H-carbazol-1-amine | HCID 597879 | — |
| Reactant | 2-Chloro-5-propylpyrimidine | HCID 2735784 | — |
| Product | HCID 11338120 | HCID 11338120 | — |
Reaction Steps
6-Bromo-N-(5-propylpyrimidin-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 5-propyl-2-chloropyrimidine (0.5 mL) in a similar manner as described above to give 5 mg (5%) of a yellow solid. 1H-NMR (DMSO-d6): δ 10.86 (s, 1H), 8.17 (s, 2H), 7.53 (s, 1H), 7.30 (d, 1H), 7.22 (d, 1H), 7.10 (d, 1H), 5.30-5.23 (m, 1H), 2.63-2.56 (m, 2H), 2.36 (t, 2H), 2.06-1.96 (m, 2H), 1.84-1.73 (m, 2H), 1.56-1.47 (m, 2H), 0.88 (t, 3H); MS m/z (M−1) 383, 385.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351733B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-13c3b7ca921441c3ab297a5cfdd2f1ec |
| Source note | uspto-grants-2008_04 |