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Potassium Hydroxide → L-Phenylalanine

HRID 2254285
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2254285
C[O:2][C:3](=[O:33])[C@H:4]([CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[NH:5]C(CC1N(CC2C=CC=CC=2Cl)C(SCCC)=NC=1)=O.[OH-].[K+]>C(O)C.O>[NH2:5][C@H:4]([C:3]([OH:33])=[O:2])[CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 14797Potassium HydroxideHCID 54145803N-[{1-(2-chlorophenyl)methyl-2-propylthio-1H-imidazol-5-yl}methylcarbonyl]-L-phenylalanine methyl ester

Produkt 1

HCID 6140L-Phenylalanine

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

The methyl ester from Example 9 (i) (0.58 g, 1.2 mmol) was dissolved in ethanol (10 mL) and a solution of potassium hydroxide (0.223 g, 4 mmol) in water (4 mL) was added. This solution was stirred at room temperature for 1.5 hours. The ethanol was evaporated, the residue was diluted with water (10 mL) and the basic solution was extracted with ether. The aqueous layer was acidified to pH 3.5 with 10% hydrochloric acid solution, and the cooled suspension was then filtered, washed with water and dried in vacuum to provide 0.46 g (82%) of N-[1-(2-chlorophenyl)methyl-2-propylthio-1H-imidazol-5-yl}methylcarbonyl]-L-phenylalanine; mp 120°-121° C.

Aufarbeitung

  1. customThe ethanol was evaporated
  2. additionthe residue was diluted with water (10 mL)
  3. extractionthe basic solution was extracted with ether
  4. filtrationthe cooled suspension was then filtered
  5. washwashed with water
  6. customdried in vacuum

Quellen und Nachweise

ORD-Eintrag
ord-5a3f3693207a458b910f049270af9f40
Quelldatensatz
uspto-grants-1993_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05234917

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