Реакция #1900

ord-daf4ba5367694338ab2591f41b1c75e1

Уравнение реакции

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
Выход 99.8%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

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

Методика

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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726306uspto-grants-1998_03