Réaction #744213

Équation de réaction

1,1-dimethylethyl ((3S,4R)-3-hydroxy-1-{2-[7-(methyloxy)-2-oxo-1,5-naphthyridin-1(2H)-yl]ethyl}-4-piperidinyl)carbamate

hydrogen chloride

→

title compound

1-{2-[(3S,4R)-4-amino-3-hydroxy-1-piperidinyl]ethyl}-7-(methyloxy)-1,5-naphthyridin-2(1H)-one Dihydrochloride

Solvants

DCM

1,4-dioxane

Conditions de réaction

Traitement

1. 1
   Autrethe solvents were removed under reduced pressure
2. 2
   Autrethe residue was dried under reduced pressure overnight

Mode opératoire

1,1-dimethylethyl ((3S,4R)-3-hydroxy-1-{2-[7-(methyloxy)-2-oxo-1,5-naphthyridin-1(2H)-yl]ethyl}-4-piperidinyl)carbamate (223 mg) was dissolved in DCM (2 ml) and the solution was treated with 4M hydrogen chloride in 1,4-dioxane (2 ml). Effervescence and formation of a precipitate was observed. After 2 h, the solvents were removed under reduced pressure and the residue was dried under reduced pressure overnight, to give the title compound as a pale yellow solid (209 mg).

Source