Trifluoroacetic acid → HCID 21843640, Verbindung

HRID 507507Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 507507
C(OC(=O)[NH:7][CH2:8][CH2:9][N:10]1[CH:14](O)[CH2:13][NH:12][C:11]1=[O:16])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[NH2:7][CH2:8][CH2:9][N:10]1[CH:14]=[CH:13][NH:12][C:11]1=[O:16]

Komponenten

4

Edukt 2

HCID 6422Trifluoroacetic acidHCID 60204244[2-(5-Hydroxy-2-oxo-imidazolidin-1-yl)-ethyl]-carbamic acid tert-butyl ester

Produkt 1

HCID 21843640HCID 21843640, VerbindungAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

[2-(5-Hydroxy-2-oxo-imidazolidin-1-yl)-ethyl]-carbamic acid tert-butyl ester (7.85 g, 32 mmol) was suspended in DCM (250 mL) and a solution of TFA (100 mL) in DCM (250 mL) was added over 10 min to the stirred suspension, which dissolved. The solution was stirred for 16 h, concentrated, and azeotroped with MeCN. The resulting TFA salt of the product was dissolved in MeOH (10 mL) and purified on 50 g of SCX resin, washing with MeOH and eluting off with 2 M NH3 in MeOH. Concentration gave the product as a pale yellow oil (3.66 g, 90%). MS (M+H)+ 128.

Aufarbeitung

  1. dissolutiondissolved
  2. concentrationconcentrated
  3. customazeotroped with MeCN
  4. dissolutionThe resulting TFA salt of the product was dissolved in MeOH (10 mL)
  5. custompurified on 50 g of SCX resin
  6. washwashing with MeOH
  7. washeluting off with 2 M NH3 in MeOH
  8. concentrationConcentration

Quellen und Nachweise

ORD-Eintrag
ord-75085d2d1138445c84a01d0da1b74ba3
Quelldatensatz
uspto-grants-2010_08
Patentnummer
US07786132B2

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