Реакция #640543

ord-ff2021606e9a467586392bd68832c7ae

Уравнение реакции

CCOC(C)=O
ethyl acetate
Cc1ccccc1C(=O)Cl
orthotoluoyl chloride
CCN(CC)CC
triethylamine
NC(=O)c1ccccc1
benzamide

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with 5% citric acid, saturated sodium bicarbonate, brine
  2. 2
    Другоеdried
  3. 3
    Фильтрацияfiltered
  4. 4
    Концентрированиеconcentrated
  5. 5
    Другоеto afford 420 mg of crude material
  6. 6
    ДругоеThis was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane

Методика

To a solution of 391 mg (1 mmol) of 2R-hydroxy-3-[(2-methylpropyl)(4-aminophenyl)sulfonyl]amino-1S-(phenylmethyl)propylamine in 3 mL of anhydrous methylene chloride, was added 0.42 mL (3 mmol) of triethylamine, then at room temperature, 0.12 mL (0.9 mmol) of orthotoluoyl chloride was added. After 15 hours at room temp ethyl acetate was added, washed with 5% citric acid, saturated sodium bicarbonate, brine, dried, filtered and concentrated to afford 420 mg of crude material. This was chromatographed on 40 g of silica gel using 50% ethyl acetate/hexane to afford 368 mg of pure benzamide, N-[2R-hydroxy-3-[[(4-aminophenyl)sulfonyl](2-methylpropyl) amino]-1S-(phenylmethyl)propyl]-2-methyl, m/e=516(M+Li).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE042889E1uspto-grants-2011_11