Reaktion #316217

ord-0edd1f8b30e14d7c9ea0066e032efd63

Reaktionsgleichung

Cl
hydrochloric acid
Nc1ncccc1C=O
2-Amino-pyridine-3-carbaldehyde
CCC(=O)CBr
1-bromo-butan-2-one
[Na+].[OH-]
sodium hydroxide
CCc1nc2ncccc2cc1O
2-ethyl-[1,8]naphthyridin-3-ol
Ausbeute 74.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe suspension was hermetically sealed and, in this state
  2. 2
    Filtrationthe precipitate was then filtered
  3. 3
    WaschenThe residue was washed with water and chloroform
  4. 4
    SonstigeThe powder as the residue was dried under the reduced pressure

Vorschrift

2-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, and the precipitate was then filtered. The residue was washed with water and chloroform. The powder as the residue was dried under the reduced pressure to give 2-ethyl-[1,8]naphthyridin-3-ol (106 mg, yield 74%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07560558B2uspto-grants-2009_07