HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 8-hydroxy-1,6-Naphthyridine-7-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 8-hydroxy-1,6-naphthyridine-7-carboxylate | HCID 22346294 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-hydroxy-1,6-Naphthyridine-7-carboxylic acid | HCID 20816864 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
To a slurry of methyl 8-hydroxy-1,6-naphthyridine-7-carboxylate from Example 1, Step 2 (1.50 g, 7.35 mmol) in methanol (45 ml) was added lithium hydroxide (22.0 ml of a 1M aq. solution, 22.0 mmol) and the reaction was heated at 100° C. for 7 hrs. Upon cooling to room temperature, hydrochloric acid (22.0 ml of a 1M aq. solution, 22.0 mmol) was added and the reaction stirred for 16 hrs. The mixture was concentrated to a volume of 50 ml and neutralized with dilute NaHCO3 (pH=7). The resulting precipitate was collected by filtration and washed with water and dried in vacuo to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06841558B2 |
| Source dataset | uspto-grants-2005_01 |
| ORD ID | ord-d1e11fd50d3347c2a972d07a39605578 |
| Source note | uspto-grants-2005_01 |