Ammonium Hydroxide → 3-Hydroxy-1-adamantyl-D-glycine

HRID 29134

Reaktionsgleichung

Reaktionsgleichung von HRID 29134
C([O-])=O.[NH4+:4].[OH:5][C:6]12[CH2:15][CH:10]3[CH2:11][CH:12]([CH2:14][C:8]([C:16](=O)[C:17]([OH:19])=[O:18])([CH2:9]3)[CH2:7]1)[CH2:13]2.[OH-].[NH4+]>SC[C@H]([C@@H](CS)O)O>[NH2:4][C@@H:16]([C:8]12[CH2:14][CH:12]3[CH2:11][CH:10]([CH2:15][C:6]([OH:5])([CH2:13]3)[CH2:7]1)[CH2:9]2)[C:17]([OH:19])=[O:18]

Komponenten

5

Edukt 3

HCID 14923Ammonium HydroxideHCID 2723923Ammonium formateHCID 104661932-(3-Hydroxy-1-adamantyl)-2-oxoacetic acid

Produkt 1

HCID 102630783-Hydroxy-1-adamantyl-D-glycineAusbeute 105,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 446094D-1,4-DithiothreitolKatalysator

Versuchsvorschrift

A 266 ml solution was prepared containing ammonium formate (16.74 g, 0.2654 moles) and (3-hydroxy-adamantan-1-yl)-oxo-acetic acid (29.76 g, 0.1327 moles) and brought to pH 8.0 with 12.7 ml concentrated ammonium hydroxide. AND (372 mg, 0.561 mmoles) and dithiothreitol (81.8 mg, 0.530 mmoles) were added, then the solution was added to the bottle containing the Escherichia coli extract. The bottle was maintained at 400 on a shaker at 40 rpm. Concentrated ammonium hydroxide was added periodically to maintain pH 8.0 After 38 hours, the solution contained 31.5 grams (0.140 moles, 100% yield) (S)-amino-(3-hydroxy-adamantan-1-yl)-acetic acid as measured by HPLC analysis and no R-enantiomer of the amino acid.

Aufarbeitung

  1. additionthe solution was added to the bottle
  2. additioncontaining the Escherichia coli
  3. extractionextract
  4. temperatureThe bottle was maintained at 400 on a shaker at 40 rpm
  5. additionConcentrated ammonium hydroxide was added periodically
  6. temperatureto maintain pH 8.0 After 38 hours

Quellen und Nachweise

ORD-Eintrag
ord-fba9cc6497f849189f6520cea1fab0f0
Quelldatensatz
uspto-grants-2008_09
Patentnummer
US07420079B2

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