Oxygen → Eniluracil

温度

50 °C

A solution of 5-iodouracil (8 g, 30 mmol) in redistilled triethylamine (500 mL) and dry DMF (10 mL) was degassed with oxygen-free nitrogen for 15 minutes. Bis(triphenylophosphine)palladium (II) chloride (0.5 g), copper (I) iodide (0.5 g) and trimethylsilylacetylene (10 g, 102 mmol) were then added and the mixture was heated with stirring at 50° C. for 24 hours. The cooled reaction mixture was filtered, the filtrate evaporated to dryness and the residue dissolved in dichloromethane (500 mL). The organic solution was washed with a 2% aqueous solution of disodium EDTA (3×250 mL), water (3×200 mL), dried (Na2SO4) and evaporated to dryness. The residue was triturated with ethanol to give the first crop of the title compound. The solid filtered from the reaction mixture was also found to contain the required product but in a more impure form and so was worked up as above in a separate batch to give a second crop.

1. temperaturethe mixture was heated
2. customThe cooled reaction mixture
3. filtrationwas filtered
4. customthe filtrate evaporated to dryness
5. dissolutionthe residue dissolved in dichloromethane (500 mL)
6. washThe organic solution was washed with a 2% aqueous solution of disodium EDTA (3×250 mL), water (3×200 mL)
7. dry with materialdried (Na2SO4)
8. customevaporated to dryness
9. customThe residue was triturated with ethanol

ORDレコード

ord-73bd4597af6043f6b1b6d110f0f0d22f

出典データセット

uspto-grants-2010_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07704971B2