Reacción #1245068
ord-bbb9581c6a214692999934708d185ec9
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1ConcentraciónThe mixture was concentrated
- 2Otrothe residue was partitioned between CH2Cl2 (50 mL) and brine (10 mL)
- 3OtroThe phases were separated
- 4Extracciónthe aqueous phase was extracted with CH2Cl2 (3×10 mL)
- 5SecadoThe combined organic extracts were dried (Na2SO4)
- 6Concentraciónconcentrated
- 7OtroPurification of the crude material by column chromatography on silica gel (25:1 CH2Cl2—CH3OH)
- 8Otroa further chromatographic purification by column chromatography on silica gel (2:1 hexanes-EtOAc) and radial chromatography on silica gel (2 mm plate, 100:1:1 CH2Cl2—CH3OH—NH4OH)
Procedimiento
To a solution of (1-tert-butoxycarbonyl-1H-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (0.409 g, 1.08 mmol) in CH3CN (5 mL) was added N,N-diisopropylethylamine (0.38 mL, 2.18 mmol) followed by a solution of ethyl 6-(bromomethyl)-2-methoxybenzoate (0.454 g, 1.66 mmol) in CH3CN (6 mL). The resultant mixture was heated to 60° C. for 22 hours then cooled to room temperature. The mixture was concentrated and the residue was partitioned between CH2Cl2 (50 mL) and brine (10 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (3×10 mL). The combined organic extracts were dried (Na2SO4) and concentrated. Purification of the crude material by column chromatography on silica gel (25:1 CH2Cl2—CH3OH) followed a further chromatographic purification by column chromatography on silica gel (2:1 hexanes-EtOAc) and radial chromatography on silica gel (2 mm plate, 100:1:1 CH2Cl2—CH3OH—NH4OH) provided 0.38 g (62%) of a white solid.