HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-bromo-N-quinolin-7-ylbenzamide → HCID 57682709, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-bromo-N-quinolin-7-ylbenzamide | HCID 831408 | — |
| Reactant | 2-Acetylphenylboronic acid | HCID 2734309 | — |
| Product | HCID 57682709 | HCID 57682709 | — |
Reaction Steps
Using the procedure outlined in Example 58, the title compound was prepared from 4-bromo-N-quinolin-7-ylbenzamide (Example 82) (50 mg, 0.153 mmol) and 2-acetyl-phenylboronic acid (28 mg, 0.17 mmol) as an off -white solid. 1H NMR (400 MHz, CDCl3) δ (ppm): 8.92 (dd, 1H), 8.21 (d, 1H), 8.20 (s, 1H), 8.14 (d, 1H), 8.10 (dd, 1H), 7.86 (d, 1H), 7.63 (dd, 1H), 7.57 (td, 1H), 7.48 (m, 3H), 7.40 (dd, 1H), 7.35 (dd, 1H), 3.85 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-da7996d07a144ea783a104881ccbd863 |
| Source note | uspto-grants-2009_05 |