HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminoquinoline → 2-(2,6-Dimethylphenyl)-1H-indole-6-carboxylic acid quinolin-2-ylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminoquinoline | HCID 11379 | — |
| Reactant | methyl 2-(2,6-dimethylphenyl)-1H-indole-6-carboxylate | HCID 66966102 | — |
| Product | 2-(2,6-Dimethylphenyl)-1H-indole-6-carboxylic acid quinolin-2-ylamide | HCID 66965308 | — |
Reaction Steps
The title compound was prepared from methyl 2-(2,6-dimethylphenyl)-1H-indole-6-carboxylate and 2-aminoquinoline analogous to Example 3-6. 1H NMR (DMSO-d6, 400 MHz) δ 11.60 (s, 1H), 11.01 (s, 1H), 8.40 (s, 2H), 7.95 (d, J=7.83 Hz, 1H), 7.89 (d, J=8.46 Hz, 1H), 7.80 (d, J=9.60 Hz, 1H), 7.74 (t, 1H), 7.65 (d, J=8.34 Hz, 1H), 7.52 (t, 1H), 7.28 (m, 1H), 7.19 (d, J=7.45 Hz, 1H), 6.44 (s, 1H), 2.15 (s, 6H). MS (m/z) 392.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08222248B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-9acdfa3456f84e37b06c1b8200e0fe1c |
| Source note | uspto-grants-2012_07 |