Ethanol → 6-(4-Amino-phenoxy)-pyrimidin-4-ylamine

Temperatur

80 °C

After suspending 6-(4-nitrophenoxy)pyrimidin-4-ylamine (306 mg, 1.32 mmol), iron powder (369 mg, 6.60 mmol) and ammonium chloride (706 mg, 13.2 mmol) in an ethanol (20 ml)-water (5 ml) mixed solvent, the suspension was heated and stirred at 80° C. for 20 minutes. After completion of the reaction, the reaction mixture was filtered with celite and washed in ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate, the drying agent was filtered off and the filtrate was concentrated to obtain the title compound (266 mg, 1.32 mmol, 100%) as light yellow crystals.

1. additionmixed solvent
2. temperaturethe suspension was heated
3. customAfter completion of the reaction
4. filtrationthe reaction mixture was filtered with celite
5. washwashed in ethyl acetate
6. washThe organic layer was washed with saturated saline
7. dry with materialdried over anhydrous magnesium sulfate
8. filtrationthe drying agent was filtered off
9. concentrationthe filtrate was concentrated

ORD-Eintrag

ord-70fc1be8da734c77889dfbeea50a84f3

Quelldatensatz

uspto-grants-2013_02

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08372981B2