Hydrochloric Acid → HCID 18966366, Verbindung

Temperatur

-70 °C

n-Butyl-lithium (1.6M solution in hexane) (7.0 ml, 11.2 mmol, 1.1 equiv.) was added dropwise at below -60° C. to a solution of 1-(2-methoxyphenyl)-4-(2-pyridylethyl)piperazine base (3.00 g, 10.1 mmol) in anhydrous THF (20 ml). The resulting orange-red solution was stirred for a further 0.25 h at -70° C. then quenched with a solution of ortho-anisaldehyde (1.5 g, 11.0 mmol) in anhydrous THF (2 ml). The reaction mixture was poured into water (50 ml) and extracted with dichloromethane (2×75 ml). The organic extract was washed (brine), dried (Na2SO4) and concentrated in vacuo. The residue was subjected to chromatography (SiO2 :Et2O) to give the first Rf diastereoisomer as a white foam which was dissolved in isopropanol (20 ml) and acidified with ethanolic hydrogen chloride to afford the first diastereoisomer of the title compound as the trihydrochloride (227 mg), m.p. 140°-145° C. (Found: C,57.7;H,6.5;N,7.8 C26H31N3O3.3HCl requires C,57.5;H,6.3;N,7.7%).

1. extractionextracted with dichloromethane (2×75 ml)
2. extractionThe organic extract
3. washwas washed (brine)
4. dry with materialdried (Na2SO4)
5. concentrationconcentrated in vacuo
6. customto give the first Rf diastereoisomer as a white foam which

ORD-Eintrag

ord-f2564d9371f24ee9b7f9e11caa00f9fa

Quelldatensatz

uspto-grants-1994_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US05346896