Reacción #1900
ord-daf4ba5367694338ab2591f41b1c75e1
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added dropwise to the solution
- 2workup.STIRRINGThe mixture was stirred for one hour at room temperature
- 3Concentraciónconcentrated
- 4workup.ADDITIONAfter the addition of 200 ml of 1N hydrochloric acid
- 5Extracciónthe concentrate was extracted with 200 ml of ethyl acetate
- 6LavadoThe organic layer was washed with a saturated sodium bicarbonate aqueous solution
- 7Secadodried over anhydrous magnesium sulfate
- 8OtroThe solvent was evaporated off under reduced pressure
- 9OtroThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=1:1)
Procedimiento
In 200 ml of tetrahydrofuran was dissolved 14.7 g of trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid obtained in Example 2 and 4.51 ml of N-methylmorpholine. To the solution was added 3.92 ml of ethyl chlorocarbonate at -10° C.; the mixture was then stirred for 15 minutes. After the addition of 3.86 g of sodium borohydride, 200 ml of methanol was added dropwise to the solution. The mixture was stirred for one hour at room temperature and then concentrated. After the addition of 200 ml of 1N hydrochloric acid, the concentrate was extracted with 200 ml of ethyl acetate. The organic layer was washed with a saturated sodium bicarbonate aqueous solution and dried over anhydrous magnesium sulfate. The solvent was evaporated off under reduced pressure. The residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=1:1) to yield 14.2 g of trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-ethanol as colorless crystals, m.p. 157° to 159° C.