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Hydrochloric Acid → N-benzoyl-L-alanyl-L-phenylalanine methyl ester

HRID 434133
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 434133
Cl.[CH3:2][O:3][C:4](=[O:14])[C@H:5]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[NH2:6].CN1CCOCC1.[C:22]([N:30]1[C@@H:34]([CH3:35])[C:33](=O)[O:32]C1=O)(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C(N[C@H](C(O)=O)C)(=O)C1C=CC=CC=1.Cl>O1CCCC1>[CH3:2][O:3][C:4](=[O:14])[C@H:5]([CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[NH:6][C:33](=[O:32])[C@H:34]([CH3:35])[NH:30][C:22](=[O:29])[C:23]1[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 79724-MethylmorpholineHCID 75736Methyl L-phenylalaninate hydrochlorideHCID 709778N-benzoyl-L-alanineHCID 9855930(S)-3-benzoyl-4-methyl-2,5-oxazolidinedione

Produkt 1

HCID 59119734N-benzoyl-L-alanyl-L-phenylalanine methyl ester
Ausbeute 65 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

L-Phenylalanine methyl ester hydrochloride (518 mg, 2.4 mmol) was suspended in tetrahydrofuran (12 mL), and at 0° C., N-methylmorpholine (242 mg, 2.4 mmol) was added, followed by stirring for 20 minutes. (S)-3-Benzoyl-4-methyl-2,5-oxazolidinedione (N-benzoyl-L-alanine-NCA (438 mg, 2 mmol) was added as crystals at 0° C. After the resulting mixture was stirred for 15 minutes, the mixture was allowed to rise in temperature to room temperature, at which the mixture was stirred for 15 minutes. The reaction mixture was poured into 1 N hydrochloric acid (25 mL), followed by extraction with ethyl acetate (25 mL). The organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate (25 mL) and a saturated aqueous solution of sodium chloride (25 mL), and was then dried over anhydrous magnesium sulfate. The organic layer was concentrated under reduced pressure. The resulting white solid was washed with hexane-ethyl acetate to afford the title compound (462 mg, 65%) as white crystals.

Aufarbeitung

  1. stirringAfter the resulting mixture was stirred for 15 minutes
  2. customto rise in temperature to room temperature, at which
  3. stirringwas stirred for 15 minutes
  4. extractionfollowed by extraction with ethyl acetate (25 mL)
  5. washThe organic layer was washed successively with a saturated aqueous solution of sodium hydrogencarbonate (25 mL)
  6. dry with materiala saturated aqueous solution of sodium chloride (25 mL), and was then dried over anhydrous magnesium sulfate
  7. concentrationThe organic layer was concentrated under reduced pressure
  8. washThe resulting white solid was washed with hexane-ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-2d928e96782b4168bd8fe66f854af487
Quelldatensatz
uspto-grants-2003_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06670447B2

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