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Isobutyl chloroformate → meso-DAP (D)GlyOH

HRID 1462113
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1462113
[NH2:1][C@@H:2]([C:4]([OH:6])=[O:5])[CH3:3].[CH3:7][Si](C([Si](C)(C)C)C(N)=O)(C)C.ClC(OCC(C)C)=O.C[Si]([O:31][C:32](=[O:36])[C@@H:33]([CH3:35])[NH2:34])(C)C>C(Cl)Cl.CN(C)C=O>[CH2:7]([CH2:35][C@H:33]([NH2:34])[C:32]([OH:31])=[O:36])[CH2:3][C@@H:2]([NH2:1])[C:4]([OH:6])=[O:5].[NH2:1][CH2:2][C:4]([OH:6])=[O:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 62365Isobutyl chloroformateHCID 71080D-AlanineHCID 11708267BistrimethylsilylacetamidHCID 22818877D-alanine trimethylsilyl ester

Produkt 1

HCID 87968512meso-DAP (D)GlyOH

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6228
Dimethylformamide
Lösungsmittel
HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a suspension of D-alanine (2.89 g) in a mixture of methylene chloride (30 ml) and dimethylformamide (12 ml) was added bis(trimethylsilyl)acetamide (30 ml) and the mixture was stirred for 15 hours at room temperature to give a clear solution. To a solution of the mixed anhydride of Z-(L)-Boc-(D)-mesoDAP-(D)-NHNHBoc (1) (13.45 g) in methylene chloride (140 ml), prepared by adding N-methylmorphorine (3.03 g) and isobutyl chloroformate (4.10 g) at -15° and stirring the mixture for 40 minutes at the same temperature, was added in one portion the above solution of D-alanine trimethylsilyl ester at -40° C. Then the reaction mixture was allowed to warm up to 0° C. and stirred for 2 hours. The reaction mixture was evaporated and the residue was dissolved in water, acidified with diluted hydrochloric acid and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated to give a white powder (12.25 g) of Z-(L)-Boc-(D)-mesoDAP-(D)-NHNHBoc-(L)-D-AlaOH (2).

Aufarbeitung

  1. customto give a clear solution
  2. stirringstirring the mixture for 40 minutes at the same temperature
  3. temperatureto warm up to 0° C.
  4. stirringstirred for 2 hours
  5. customThe reaction mixture was evaporated
  6. dissolutionthe residue was dissolved in water
  7. extractionextracted with ethyl acetate
  8. washThe extract was washed with water
  9. dry with materialdried over magnesium sulfate
  10. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-5ceff8ac503f41aabc12ca8929206146
Quelldatensatz
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04458078

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