HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 5-bromo-8-hydroxy-1,6-naphthyridine-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 8-hydroxy-1,6-naphthyridine-7-carboxylate | HCID 22346294 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-bromo-8-hydroxy-1,6-naphthyridine-7-carboxylate | HCID 22343006 | — |
Reaction Steps
To a solution of methyl 8-hydroxy-1,6-naphthyridine-7-carboxylate from Example 1 Step 2 (5.0 g, 24.49 mmol) in CH2Cl2 (100 ml) at room temperature was added N-bromo succinimide (4.36 g, 24.49 mmol). The reaction was stirred for 1 hr. The solids were collected by filtration and dried in vacuo to afford the title compound as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921759B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-50658384c79e4c8a8fe54e588451ee6b |
| Source note | uspto-grants-2005_07 |