Réaction #1900

ord-daf4ba5367694338ab2591f41b1c75e1

Équation de réaction

CC(C)(C)CN1C(=O)[C@@H](CC(=O)O)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid
CN1CCOCC1
N-methylmorpholine
[BH4-].[Na+]
sodium borohydride
CCOC(=O)Cl
ethyl chlorocarbonate
CC(C)(C)CN1C(=O)[C@@H](CCO)O[C@H](c2ccccc2Cl)c2cc(Cl)ccc21
trans-7-chloro-5-(2-chlorophenyl)-1-neopentyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-ethanol
Rendement 99.8%

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwas added dropwise to the solution
  2. 2
    workup.STIRRINGThe mixture was stirred for one hour at room temperature
  3. 3
    Concentrationconcentrated
  4. 4
    workup.ADDITIONAfter the addition of 200 ml of 1N hydrochloric acid
  5. 5
    Extractionthe concentrate was extracted with 200 ml of ethyl acetate
  6. 6
    LavageThe organic layer was washed with a saturated sodium bicarbonate aqueous solution
  7. 7
    Séchagedried over anhydrous magnesium sulfate
  8. 8
    AutreThe solvent was evaporated off under reduced pressure
  9. 9
    AutreThe residue was purified by silica gel column chromatography (eluent, hexane:ethyl acetate=1:1)

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05726306uspto-grants-1998_03