Реакция #416731

ord-29a1926728084fa1aaad95e46d3ea39c

Растворители

Условия реакции

Температура
0°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.STIRRINGThe mixture was stirred for 20 h while the temperature of the mixture
  2. 2
    Другоеgradually came to room temperature
  3. 3
    ДругоеConcentration of the reaction mixture under reduced pressure gave an oil
  4. 4
    ПромывкаThe solution was washed with 1N HCl, 1N NaHCO3 and H2O
  5. 5
    Сушкаdried (Na2SO4 /MgSO4)
  6. 6
    Концентрированиеconcentrated to dryness
  7. 7
    Другоеto give an oil

Методика

Tetrapeptide H-Ser(Bzl)-Gly-Leu-Gly-OCH3 : HCl.H-Leu-Gly-OCH3 (12.2 g, 51.3 mmol) was dissolved in DMF (200 mL). DIEA (24 mL, 139.8 mmol) was added to the solution. This first solution was cooled to 0° C. A second solution of Boc-Ser-(Bzl)-Gly-OH (16.42 g, 46.6 mmol) and DPPA (14.1 g, 51.26 mmol) in DMF (122 mL) was added with stirring to the first solution. The mixture was stirred for 20 h while the temperature of the mixture gradually came to room temperature. Concentration of the reaction mixture under reduced pressure gave an oil. The oil was dissolved in EtOAc. The solution was washed with 1N HCl, 1N NaHCO3 and H2O, dried (Na2SO4 /MgSO4) and concentrated to dryness to give an oil. Trituration of the latter oil with Et2O-hexane yielded Boc-Ser(Bzl-Gly-Leu-Gly-OCH3 as a solid (23.82 g). The latter compound (28.82 g) was dissolved in 1N HCl in glacial acetic acid (100 mL). The mixture was stirred at room temperature for 1 h and then concentrated under reduced vacuum to give an oil. Trituration of the oil with Et2O afforded the tetrapeptide as a solid (19.71 g, HCl salt).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US04891358uspto-grants-1990_01