Potassium Hydroxide → N-[3-carboxy-2-(2-methylpropyl)propanoyl]-O-methyl-L-tyrosine N-methylamide

HRID 1252379Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1252379
[CH3:1][NH:2][C:3](=[O:28])[C@H:4]([CH2:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][CH3:27])=[CH:22][CH:21]=1)[NH:5][C:6](=[O:18])[CH:7]([CH2:14][CH:15]([CH3:17])[CH3:16])[CH2:8][C:9]([O:11]CC)=[O:10].[OH-].[K+]>CO>[CH3:1][NH:2][C:3](=[O:28])[C@H:4]([CH2:19][C:20]1[CH:21]=[CH:22][C:23]([O:26][CH3:27])=[CH:24][CH:25]=1)[NH:5][C:6](=[O:18])[CH:7]([CH2:14][CH:15]([CH3:16])[CH3:17])[CH2:8][C:9]([OH:11])=[O:10]

Komponenten

4

Edukt 2

HCID 14797Potassium HydroxideHCID 14303040N-[3-(ethoxycarbonyl)-2-(2-methylpropyl)propanoyl]-O-methyl-L-tyrosine N-methylamide

Produkt 1

HCID 14303042N-[3-carboxy-2-(2-methylpropyl)propanoyl]-O-methyl-L-tyrosine N-methylamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

N-[3-(Ethoxycarbonyl)-2-(2-methylpropyl)propanoyl]-O-methyl-L-tyrosine N-methylamide (4.7 g., 0.012 mol.) was suspended in methanol (25 mls.) containing potassium hydroxide solution (12 mls. of 1M). The mixture was stirred overnight and the solvent was removed by evaporation in vacuo to yield a gum. The gum was partitioned between diethyl ether (50 mls.) and sodium bicarbonate solution (50 mls.). The aqueous phase was separated, washed with ethyl ether (50 mls.) and adjusted to pH 2 by the addition of dilute hydrochloric acid. The aqueous mixture was extracted with dichloromethane (3×100 mls.) and the extracts combined and then dried over anhydrous sodium sulfate. The solvent was removed by evaporation in vacuo to yield a gum (3.3 g.). The gum was recrystallized from a mixture of dichloromethane and hexane to yield N-[3-carboxy-2-(2-methylpropyl)propanoyl]-O-methyl-L-tyrosine N-methylamide as a white solid which was a mixture of two diastereomers. (m.p. 92°-96° C.

Aufarbeitung

  1. customthe solvent was removed by evaporation in vacuo
  2. customto yield a gum
  3. customThe gum was partitioned between diethyl ether (50 mls.) and sodium bicarbonate solution (50 mls.)
  4. customThe aqueous phase was separated
  5. washwashed with ethyl ether (50 mls.)
  6. additionadjusted to pH 2 by the addition of dilute hydrochloric acid
  7. extractionThe aqueous mixture was extracted with dichloromethane (3×100 mls.)
  8. dry with materialdried over anhydrous sodium sulfate
  9. customThe solvent was removed by evaporation in vacuo
  10. customto yield a gum (3.3 g.)
  11. customThe gum was recrystallized from a mixture of dichloromethane and hexane

Quellen und Nachweise

ORD-Eintrag
ord-6a5a850b980e499c87165ef97191b3e3
Quelldatensatz
uspto-grants-1988_05
Patentnummer
US04743587

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