Water → Tri-Boc Lysine-beta-aminoethyl Ester

HRID 1040295Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1040295
[C:1]([N:8]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[C@H:9]([C:15]([OH:17])=[O:16])[CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:25](C(CN)O)([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26].[CH3:36][CH2:37][N:38]=C=NCCCN(C)C.Cl.O>ClCCl.CN(C)C1C=CN=CC=1>[NH2:38][CH2:37][CH2:36][O:16][C:15](=[O:17])[C@:9]([C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])([CH2:10][CH2:11][CH2:12][CH2:13][NH2:14])[N:8]([C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[C:1]([O:3][C:4]([CH3:5])([CH3:7])[CH3:6])=[O:2]

Komponenten

7

Versuchsvorschrift

Di-Boc lysine (770 grams, 2.2 mol) was dissolved in dichloromethane (4 liters). Bocethanolamine (340 grams, 2.1 mol) was added to the solution, along with 4-dimethylaminopyridine (50 grams.) EDC-HCl (450 grams, 2.35 mol) was added and the mixture was allowed to stir overnight at room temperature. Water (2 liters) was added and the mixture was stirred for 30 minutes. The layers were separated, and the aqueous layer was extracted with dichloromethane. The combined organics were washed with saturated sodium bicarbonate, 1N HCl solution, and brine. Solvent was removed under reduced pressure to give an oil. Mass recovery was 770 grams (68% yield).

Aufarbeitung

  1. additionwas added
  2. stirringthe mixture was stirred for 30 minutes
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with dichloromethane
  5. washThe combined organics were washed with saturated sodium bicarbonate, 1N HCl solution, and brine
  6. customSolvent was removed under reduced pressure
  7. customto give an oil

Quellen und Nachweise

ORD-Eintrag
ord-02a25817089144c5a5880e63fe2b155b
Quelldatensatz
uspto-grants-2013_10
Patentnummer
US08552217B2

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