Реакция #1994225

ord-5ccfbe55755d4cbd92076028465e5564

Уравнение реакции

Cl
HCl
CCCN(CCc1cccs1)[C@H]1CCc2c(O)cccc2C1.Cl
Rotigotine HCl
CC(C)(C)OC(=O)NCC(=O)O
Boc-Glycine-OH
C(=NC1CCCCC1)=NC1CCCCC1
DCC
CC(C)(C)OC(=O)NCC(=O)O.CCCN(CCc1cccs1)[C@H]1CCc2c(O)cccc2C1
Boc-Gly Rotigotine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto give a suspension
  2. 2
    ФильтрацияThe mixture was filtered
  3. 3
    Фильтрацияusing filter paper
  4. 4
    ДругоеThe layers were separated
  5. 5
    Экстракцияthe aqueous phase was extracted with 7 mL of dichloromethane
  6. 6
    ПромывкаThe combined organic phases were washed with water
  7. 7
    Сушкаwith brine, dried over Na2SO4
  8. 8
    Фильтрацияfiltered
  9. 9
    Концентрированиеconcentrated
  10. 10
    Другоеa rotary evaporator
  11. 11
    Другоеdried in vacuo
  12. 12
    Другоеto give a crude pale yellow solid
  13. 13
    Фильтрацияfiltered on a glass frit
  14. 14
    Промывкаwashed with diethyl ether
  15. 15
    Другоеdried in vacuo

Методика

Rotigotine HCl (1.2 g, 3.41 mmol) and Boc-Glycine-OH (1.195 g, 6.82 mmol) were dissolved in dichloromethane (150 ml) to give a suspension. After addition of DMAP (0.625 g, 5.11 mmol) and DCC (1.407 g, 6.82 mmol), the mixture was stirred for 16 hours at room temperature. The mixture was filtered using filter paper and the filtrate was quenched with 51 mL of 0.1 N HCl (5.11 mmol). The layers were separated and the aqueous phase was extracted with 7 mL of dichloromethane. The combined organic phases were washed with water and then with brine, dried over Na2SO4, filtered, concentrated using a rotary evaporator, and dried in vacuo to give a crude pale yellow solid. The crude material was stirred with diethyl ether (50 mL) for 30 minutes, filtered on a glass frit, washed with diethyl ether, and dried in vacuo to give a pale yellow powder Boc-Gly-Rotigotine.HCl (1.258 g, 75% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08597633B2uspto-grants-2013_12