Water → 6-(2,4-Dimethoxyphenyl)-1-(2-hydroxyethyl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one

Temperatur

85 °C

To a solution of (Z)-methyl 3-(2,4-dimethoxyphenyl)-3-((2-hydroxyethyl)amino)acrylate (9.50 g, 33.77 mmol) in 2-MeTHF (100 mL) was added (trimethylsilyl)isothiocyanate (23.80 mL, 168.79 mmol), and the reaction mixture was heated at 85° C. After stirring overnight, the reaction mixture was cooled, extracted with an aqueous 1N NaOH solution (1×250 mL, then 1×50 mL), the combined aqueous layers were washed with CH2Cl2 (2×50 mL) and the aqueous phase acidified to pH 4 with concentrated HCl. The resulting solids were filtered, washed with water (2×50 mL) and dried under N2 overnight to give a light yellow powder. The product was dissolved in DMF (70 mL) at 90° C., and then water (80 mL) was added to this hot solution. After allowing to cool to room temperature and stirring overnight, the solids were collected by vacuum filtration, washed with water and dried under high vacuum to provide the title compound (6.7 g, 61%) as an off-white powder.

1. temperaturethe reaction mixture was cooled
2. extractionextracted with an aqueous 1N NaOH solution (1×250 mL
3. wash1×50 mL), the combined aqueous layers were washed with CH2Cl2 (2×50 mL)
4. filtrationThe resulting solids were filtered
5. washwashed with water (2×50 mL)
6. customdried under N2 overnight
7. customto give a light yellow powder
8. temperatureto cool to room temperature
9. stirringstirring overnight
10. filtrationthe solids were collected by vacuum filtration
11. washwashed with water
12. customdried under high vacuum

ORD-Eintrag

ord-ab1fb71e3e024d4e9b96131d81a92d9a

Quelldatensatz

uspto-grants-2014_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08835449B2