Reaktion #66678
ord-8c06519b6f364e26b61c9ee879ec780f
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeExcess Brederick's reagent was removed under reduced pressure
- 2workup.DISSOLUTIONThe residue was dissolved in anhydrous EtOH (10 ml)
- 3TemperaturThe reaction mixture was heated at 80° C. for 18 hrs
- 4Sonstigepartitioned between EtOAc and water
- 5TrocknenThe combined organic extracts were dried over Na2SO4
- 6Filtrationfiltered
- 7Einengenconcentrated
- 8Temperaturheated to 120° C. for 10 hrs
- 9Extraktionextracted into EtOAc
- 10TrocknenThe combined organic extracts were dried over Na2SO4
- 11Filtrationfiltered
- 12Einengenconcentrated
Vorschrift
A mixture of (2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-acetonitrile (0.27 g, 0.94 mmol) and Brederick's reagent (0.35 g, 2.01 mmol) was heated at 100° C. for 2 hrs. Excess Brederick's reagent was removed under reduced pressure. The residue was dissolved in anhydrous EtOH (10 ml) and aniline HCl (0.38 g, 2.93 mmol) was added. The reaction mixture was heated at 80° C. for 18 hrs and partitioned between EtOAc and water. The combined organic extracts were dried over Na2SO4, filtered and concentrated. Guanidine carbonate (0.27 g, 1.49 mmol) and NMP (10 ml) were added and heated to 120° C. for 10 hrs. The reaction mixture was poured into water and extracted into EtOAc. The combined organic extracts were dried over Na2SO4, filtered and concentrated. Flash chromatography on silica (3% MeOH in methylene chloride with 0.1% NH4OH) gave 5-(2-Isopropyl-4-methoxy-5-thiazol-4-yl-phenoxy)-pyrimidine-2,4-diamine (0.15 g, 68%) as a solid. (M+H)=358.