ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE
ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Basic information
- Product Name:
- ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE
- Synonyms:
-
- ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE
- 4-Hydroxy-5-pyrimidineacetic acid ethyl ester
- 5-Pyrimidineaceticacid, 3,4-dihydro-4-oxo-, ethyl ester
- ethyl 2-(6-oxo-1,6-dihydropyriMidin-5-yl)acetate
- 2-(6-oxo-1H-pyrimidin-5-yl)acetic acid ethyl ester
- ethyl 2-(6-oxo-1H-pyrimidin-5-yl)acetate
- ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE ISO 9001:2015 REACH
- CAS:
- 6214-46-6
- MF:
- C8H10N2O3
- MW:
- 182.18
- EINECS:
- 604-604-1
- Product Categories:
-
- Heterocycle-Pyrimidine series
- Mol File:
- 6214-46-6.mol
ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Chemical Properties
- Melting point:
- 155-156 °C
- Density
- 1.27±0.1 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 8.62±0.40(Predicted)
- Appearance
- White to off-white Solid
ETHYL2-(4-HYDROXYPYRIMIDIN-5-YL)ACETATE Usage And Synthesis
Synthesis
3473-63-0
5472-38-8
6214-46-6
The ethanolic solution of sodium ethoxide was cooled to 0 °C under argon protection. Under continuous stirring, diethyl 2-formylsuccinate was slowly added. after 5 minutes, the corresponding formamidine acetate was added drop by drop while maintaining the condition of 0°C. Subsequently, the reaction mixture was warmed up to room temperature and stirred continuously for 3 days. After completion of the reaction, 5% aqueous hydrogen chloride solution was added and stirring was continued for 30 minutes. After addition of appropriate amount of water, ethanol was removed by distillation under reduced pressure at 30 °C. Finally, the precipitate was collected by filtration to afford the target product ethyl 4-hydroxy-5-pyrimidineacetate (Compound 1, where X = H, Me, Ph, SMe; Y = H, R1 = Et).
References
[1] Monatshefte fur Chemie, 2016, vol. 147, # 4, p. 767 - 773
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