HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-chloro-6-methoxy-1,5-naphthyridine-3-carboxylate | HCID 23209173 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid | HCID 67255572 | 96.1% |
Reaction Steps
Sodium hydroxide (5.86 g, 140.6 mmol, 2.5 eq) is added protionwise at room temperature to a stirred solution of 4-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid ethyl ester (15.0 g, 56.25 mmol, 1.0 eq) in tetrahydrofuran (150 mL) and water (80 mL). After 15 hours stirring at room temperature, tetrahydrofuran is removed, the aqueous layer is cooled down to 0° C. and the pH is adjusted to 3 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-chloro-6-methoxy-[1,5]naphthyridine-3-carboxylic acid as a light red solid (12.9 g, 96% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08927541B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-4bd5d85cc64c49588f4e0753ddfb16f0 |
| Source note | uspto-grants-2015_01 |