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Iodine chloride → 6-Chloro-5-iodopyrimidin-4-amine

HRID 1052354
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1052354
[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH2:8])[CH:3]=1.[I:9]Cl>CN(C)C=O>[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH2:8])[C:3]=1[I:9]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 24640Iodine chlorideHCID 2380124-Amino-6-chloropyrimidine

Produkt 1

HCID 468558336-Chloro-5-iodopyrimidin-4-amineAusbeute 72 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Reaktionsbedingungen

Temperatur
45 °C

Versuchsvorschrift

To a solution of 3.03 g (23.39 mmol) of 6-chloropyrimidin-4-amine in 60 mL of dimethylformamide was added dropwise a solution of iodine monochloride (2.34 mL, 46.70 mmol) in 40 mL of dimethylformamide. Then the mixture was stirred at 45° C. overnight. The solvent was evaporated under reduced pressure and the residue was partitioned between dichloromethane and a 4% aqueous solution of sodium bicarbonate. The organic layer was washed with water and brine, dried over magnesium sulphate, filtered and the solvent was removed in vacuum. The product was purified by flash chromatography (0% to 20%, methanol-dichloromethane) to obtain 4.28 g (72% yield) of the title compound.

Aufarbeitung

  1. customThe solvent was evaporated under reduced pressure
  2. customthe residue was partitioned between dichloromethane
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customthe solvent was removed in vacuum
  7. customThe product was purified by flash chromatography (0% to 20%, methanol-dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-8ee1ac66138d4b39a5f3ea2a31b43c64
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09388189B2

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