HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1373560Erstellt: 26. Oktober 2026
Sodium triacetoxyborohydride → 7-{4-[4-(5-Chloro-2-isopropoxy-phenyl)-piperazin-1-yl]-butoxy}-1H-[1,8]naphthyridin-2-one
https://huagongshe.com/reaction/1373560
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | 1-(5-Chloro-2-isopropoxy-phenyl)-piperazine | HCID 21073166 | — |
| Edukt | 4-(7-Oxo-7,8-dihydro-1,8-naphthyridin-2-yloxy)butanal | HCID 21073380 | — |
| Lösungsmittel | 1,1-Dichloroethane | HCID 6365 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 7-{4-[4-(5-Chloro-2-isopropoxy-phenyl)-piperazin-1-yl]-butoxy}-1H-[1,8]naphthyridin-2-one | HCID 21073710 | 39,3% |
Reaktionsschritte
To a suspension of 4-(7-oxo-7,8-dihydro-[1,8]naphthyridin-2-yloxy)-butyraldehyde (0.206 g, 0.887 mmol, 1 eq) and 1-(5-chloro-2-isopropoxy-phenyl)-piperazine (0.328 g, 0.977 mmol, 1.1 eq) in dichloroethane (5 mL) was added NaBH(OAc)3 (0.535 g, 2.524 mmol, 2.84 eq). The slurry was allowed to stir overnight at room temperature (18 h). Analysis by HPLC showed reaction mostly complete. The mixture was diluted with Ethyl Acetate and quenched with saturated NaHCO3. The organic phase was washed with brine, dried over Na2SO4, filtered and evaporated in vacuo. Purification by silica gel chromatography (2% MeOH/CH2Cl2) followed by formation of the HCl salt using 1N HCl in ether provided the title compound (0.164 g, 39%). MS: APCI: M+1: 471.2 (Exact Mass: 470.21).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07160888B2 |
|---|
| Quelldatensatz | uspto-grants-2007_01 |
|---|
| ORD ID | ord-f603048e6346468d8f33df7451b7959b |
|---|
| Quellennotiz | uspto-grants-2007_01 |
|---|