HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 4-Benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid | HCID 67255572 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acid | HCID 67255027 | 98% |
Reaction Conditions
| Temperature | -40 °C |
|---|
Reaction Steps
Benzyl alcohol (5.78 g, 53.43 mmol, 2.5 eq) is added at −45° C. to a stirred solution of 4-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid (5.1 g, 21.37 mmol, 1.0 eq) in N,N-dimethylformamide (100 mL), followed by sodium hydride (2.46 g, 53.43 mmol, 2.5 eq). After 2 hours stirring at −40° C. and 24 hours stirring at room temperature, the reaction mixture is quenched with ice water, the pH is adjusted to 3-4 by the addition of a 2N hydrochloric acid aqueous solution. The resulting precipitate is collected by filtration, washed with water and dried under high vacuum to afford 4-benzyloxy-6-methoxy-[1,5]naphthyridine-3-carboxylic acid as a light red solid (6.5 g, 98% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120822B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-ab523a7367f64468b534eae6e3c21a4d |
| Source note | uspto-grants-2015_09 |