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Sulfuric acid magnesium salt (1:1) → (2S,3S)-N-[(3,4-methylenedioxy)phenyl]-3-azido-2-hydroxyheptanamide

HRID 1698433
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1698433
[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([NH:10][C:11]([C@@H:13]3[C@@H:15]([CH2:16][CH2:17][CH2:18][CH3:19])[O:14]3)=[O:12])=[CH:4][C:3]=2[O:2]1.[N-:20]=[N+:21]=[N-:22].[Na+].S([O-])([O-])(=O)=O.[Mg+2]>CO>[CH2:1]1[O:9][C:8]2[CH:7]=[CH:6][C:5]([NH:10][C:11](=[O:12])[C@@H:13]([OH:14])[C@@H:15]([N:20]=[N+:21]=[N-:22])[CH2:16][CH2:17][CH2:18][CH3:19])=[CH:4][C:3]=2[O:2]1
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Komponenten

5

Edukt 3

HCID 24083Sulfuric acid magnesium salt (1:1)HCID 33557Sodium AzideHCID 86618963(2S-trans)-N-[(3,4-methylenedioxy)phenyl]-3-butyloxiranecarboxamide

Produkt 1

HCID 59655561(2S,3S)-N-[(3,4-methylenedioxy)phenyl]-3-azido-2-hydroxyheptanamideAusbeute 70,1 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887
Methanol
Lösungsmittel

Versuchsvorschrift

30 ml of a methanol suspension containing 484 mg (1.84 mmol) of (2S-trans)-N-[(3,4-methylenedioxy)phenyl]-3-butyl-oxiranecarboxamide, 239 mg (3.68 mmol) of sodium azide and 228 mg (1.89 mmol) of anhydrous magnesium sulfate was refluxed for 5 hours. After the temperature of the reaction mixture was returned to room temperature, the reaction mixture was concentrated under reduced pressure, ethyl acetate was added to the concentrate, and the resulting mixture was washed successively with water, and then, with a saturated NaCl solution. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified by silica gel column chromatography to obtain 395 mg (Yield: 70%) of the title compound.

Aufarbeitung

  1. temperaturewas refluxed for 5 hours
  2. customwas returned to room temperature
  3. concentrationthe reaction mixture was concentrated under reduced pressure, ethyl acetate
  4. additionwas added to the concentrate
  5. washthe resulting mixture was washed successively with water
  6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  7. customthe solvent was removed under reduced pressure
  8. customThe residue was purified by silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-51df6d3228cb439490c0d62d0428e647
Quelldatensatz
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08163943B2

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