HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Aminoquinoline → 4-bromo-3-methoxy-N-quinolin-7-ylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Aminoquinoline | HCID 11377 | — |
| Reactant | 4-Bromo-3-methoxybenzoic acid | HCID 16215867 | — |
| Product | 4-bromo-3-methoxy-N-quinolin-7-ylbenzamide | HCID 69042670 | — |
Reaction Steps
Using the procedure outlined in Example 56, the title compound was prepared from 7-aminoquinoline (D55) (36 mg, 0.25 mmol) and 4-bromo-3-methoxybenzoic acid (69 mg, 0.3 mmol) as a white solid (84 mg). MS(ES): MH+ 357/359, M-H+ 355/357.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538121B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-68992ddd3e1e4211a90c95297ead02de |
| Source note | uspto-grants-2009_05 |