تفاعل #1994225

ord-5ccfbe55755d4cbd92076028465e5564

معادلة التفاعل

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

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto give a suspension
  2. 2
    ترشيحThe mixture was filtered
  3. 3
    ترشيحusing filter paper
  4. 4
    أخرىThe layers were separated
  5. 5
    استخلاصthe aqueous phase was extracted with 7 mL of dichloromethane
  6. 6
    غسيلThe combined organic phases were washed with water
  7. 7
    تجفيفwith brine, dried over Na2SO4
  8. 8
    ترشيحfiltered
  9. 9
    تركيزconcentrated
  10. 10
    أخرىa rotary evaporator
  11. 11
    أخرىdried in vacuo
  12. 12
    أخرىto give a crude pale yellow solid
  13. 13
    ترشيحfiltered on a glass frit
  14. 14
    غسيلwashed with diethyl ether
  15. 15
    أخرىdried in vacuo

الإجراء التجريبي

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).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08597633B2uspto-grants-2013_12