HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Bromoquinoline → N,N-Dimethyl-4-(quinolin-6-yl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Bromoquinoline | HCID 79243 | — |
| Reactant | 4-(Dimethylamino)phenylboronic acid | HCID 2734344 | — |
| Product | N,N-Dimethyl-4-(quinolin-6-yl)aniline | HCID 58362492 | — |
Reaction Steps
N,N-Dimethyl-4-(quinolin-6-yl)aniline T505 was prepared using general procedure A from 6-bromoquinoline (52 mg, 0.25 mmol) and (4-(dimethylamino)phenyl)boronic acid (41 mg, 0.25 mmol). The product T505 was obtained as a yellow solid (42 mg, 67%). 1H NMR (400 MHz, CDCl3): δ 8.85 (dd, J=4.4, 1.6 Hz, 1H), 8.15 (m. 2H), 7.97 (dd, J=8.4, 1.6 Hz, 1H), 7.92 (d, J=2.0 Hz, 1H), 7.63 (m, 2H), 7.38 (dd, J=8.4, 4.4 Hz, 1H), 6.84 (m, 2H), 3.01 (s, 6H); MS (ESI): 249 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691187B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-01d0668f435847df9de3ae93b6ad3475 |
| Source note | uspto-grants-2014_04 |