HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Ethyl-[1,6]naphthyridin-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromo-2-butanone | HCID 13156 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Aminonicotinaldehyde | HCID 2761033 | — |
| Product | 2-Ethyl-[1,6]naphthyridin-3-ol | HCID 23078399 | 48% |
Reaction Steps
4-Amino-pyridine-3-carbaldehyde (100 mg) and 1-bromo-butan-2-one (124 mg) were suspended in a 5 N aqueous sodium hydroxide solution (0.6 ml), and the suspension was hermetically sealed and, in this state, was allowed to stand for 3 days. The reaction solution was neutralized with 10% hydrochloric acid, the precipitate was then filtered, and the residue was washed with water and chloroform. The powder as the residue was dried under the reduced pressure to give 2-ethyl-[1,6]naphthyridin-3-ol (69 mg, yield 48%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07560558B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-4ed72ed1fcc042938e415882c50f640a |
| Source note | uspto-grants-2009_07 |