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Iodine chloride → 1-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-(1-azido-2-iodoethyl)uracil

HRID 732925
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 732925
[I:1]Cl.[N-:3]=[N+:4]=[N-:5].[Na+].[OH:7][CH2:8][CH:9]([CH2:22][OH:23])[CH2:10][CH2:11][N:12]1[CH:19]=[C:18]([CH:20]=[CH2:21])[C:16](=[O:17])[NH:15][C:13]1=[O:14].C(Cl)(Cl)Cl.CO>C(#N)C>[OH:7][CH2:8][CH:9]([CH2:22][OH:23])[CH2:10][CH2:11][N:12]1[CH:19]=[C:18]([CH:20]([N:3]=[N+:4]=[N-:5])[CH2:21][I:1])[C:16](=[O:17])[NH:15][C:13]1=[O:14]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 24640Iodine chlorideHCID 33557Sodium AzideHCID 100372831-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-vinyluracilHCID 21584188Chloroform methanol

Produkt 1

HCID 4903881-[4-Hydroxy-3-(hydroxymethyl)-1-butyl]-5-(1-azido-2-iodoethyl)uracilAusbeute 21,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342
Acetonitrile
Lösungsmittel
2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Iodine monochloride (50 mg, 0.3 mmol) was added slowly with stirring during a five minute period to a suspension of sodium azide (72 mg, 1.1 mmol) in dry acetonitrile (10 ml) at ice-bath temperature with stirring. This mixture was stirred for a further 5 min., a solution of 20 (66 mg, 0.275 mmol) in dry acetonitrile (40 ml) was added, the reaction mixture was maintained at 0° C. for 30 min. with stirring. The resulting red-brown colored reaction mixture was poured onto ice cold water (25 ml), the mixture was extracted with ethyl acetate (3×50 ml) and the ethyl acetate extract was washed with 5% aqueous sodium thiosulfate (30 ml). Drying the colorless ethyl acetate fraction. (Na2SO4), removal of the solvent in vacuo and purification of the residue obtained by elution from a silica gel column using chloroform:methanol (90:10, v/v) as eluent afforded 21c (24 mg, 21%) as a viscous oil.

Aufarbeitung

  1. stirringThis mixture was stirred for a further 5 min.
  2. stirringwith stirring
  3. additionThe resulting red-brown colored reaction mixture was poured onto ice cold water (25 ml)
  4. extractionthe mixture was extracted with ethyl acetate (3×50 ml)
  5. extractionthe ethyl acetate extract
  6. washwas washed with 5% aqueous sodium thiosulfate (30 ml)
  7. dry with materialDrying the colorless ethyl acetate fraction
  8. custom(Na2SO4), removal of the solvent
  9. customin vacuo and purification of the residue
  10. customobtained by elution from a silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-468575b97a7245ec9d3b434003cc29c2
Quelldatensatz
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07589077B2

Notizen zur Reaktion

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