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Water → HCID 57672871, Verbindung

HRID 448756
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 448756
C1(CO[C:9]([NH:11][C@H:12]([C:17]([NH:19][C@H:20]([CH2:24][OH:25])[CH:21]([CH3:23])[CH3:22])=[O:18])[CH2:13][CH:14]([CH3:16])[CH3:15])=[O:10])C=CC=CC=1.O.C(=O)([O-])[O-].[Na+].[Na+].[O:33]1[CH:37]=[CH:36][CH:35]=[C:34]1C(Cl)=O>CO.C(OCC)(=O)C.[C].[Pd]>[O:33]1[CH:37]=[CH:36][CH:35]=[C:34]1[C:9]([NH:11][C@H:12]([C:17]([NH:19][C@H:20]([CH2:24][OH:25])[CH:21]([CH3:22])[CH3:23])=[O:18])[CH2:13][CH:14]([CH3:15])[CH3:16])=[O:10]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 962WaterHCID 10340Sodium CarbonateHCID 682422-Furancarbonyl chlorideHCID 57672846N-[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-valinol

Produkt 1

HCID 57672871HCID 57672871, VerbindungAusbeute 86,3 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 178418390
HCID 178418390, Verbindung
Katalysator
HCID 887MethanolLösungsmittel
HCID 8857Ethyl AcetateLösungsmittel2×

Versuchsvorschrift

30 mg of 10% palladium-carbon was added to a solution of 350 mg (1 mmol) of N—[N-[(phenylmethoxy)carbonyl]-L-leucyl]-L-valinol obtained in Reference Example 184 in 10 ml of methanol, and the mixture was stirred under a hydrogen atmosphere at room temperature overnight. After the reaction solution was filtered, the filtrate was concentrated under reduced pressure. 10 ml of ethyl acetate, 10 ml of water and further 159 mg (1.5 mmol) of sodium carbonate were added to the residue. Under ice-cooling, a solution of 131 mg (1 mmol) of 2-furancarbonyl chloride in 3 ml of ethyl acetate was added to the mixture solution. The reaction solution was returned to room temperature and stirred overnight. The aqueous layer of the reaction solution was separately collected and it was extracted with ethyl acetate. The organic layer was combined, and after it was washed with a 10% potassium hydrogensulfate and then saturated brine, it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and ether was added to the residue to wash the crystal to obtain 268 mg (86%) of the title compound.

Aufarbeitung

  1. filtrationAfter the reaction solution was filtered
  2. concentrationthe filtrate was concentrated under reduced pressure
  3. temperatureUnder ice-cooling
  4. customwas returned to room temperature
  5. stirringstirred overnight
  6. customThe aqueous layer of the reaction solution was separately collected
  7. extractionit was extracted with ethyl acetate
  8. washafter it was washed with a 10% potassium hydrogensulfate
  9. dry with materialsaturated brine, it was dried with anhydrous sodium sulfate
  10. distillationThe solvent was distilled off under reduced pressure and ether
  11. additionwas added to the residue
  12. washto wash the crystal

Quellen und Nachweise

ORD-Eintrag
ord-cd29b7422ade46b2a3ca5b619c14eddc
Quelldatensatz
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08481725B2

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