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CAS No. : | 2078-71-9 | MDL No. : | MFCD00059080 |
Formula : | C3H8N2O2 | Boiling Point : | - |
Linear Structure Formula : | HOCH2CH2NHC(O)NH2 | InChI Key : | CLAHOZSYMRNIPY-UHFFFAOYSA-N |
M.W : | 104.11 | Pubchem ID : | 73984 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
59.4% | With sodium; In ethanol;Cooling with ice; Reflux; | Synthesis of 1-hydroxy-ethyl-6-aminouracil (compound 1) Metal sodium (2.8 g, 120 mmol) was added carefully in 90 mL of ethanol anhydride in a 200 mL mad apple-type flask with a stirrer coated with fluoropolymer in ice bath with constant stirring and was completely dissolved. Then, 6.3 g (60 mmol) of hydroxyethylurea and 6.4 mL (60 mmol) of ethylcyanoacetate were added and refluxed for seven hr. The obtained solution was filtrated, washed with ethanol, solubilized in water, neutralized with 1.0 M diluted hydrochloric acid, filtrated and provided white pellets, which were recrystallized in water and gave compound 1 as a white crystal (6.1 g, 35.6 mmol, yield: 59.4percent); 1H NMR (DMSO-d6, 400 MHz): delta 3.54 (t, 2H, NCH2CH2, 9.6 Hz), 3.83 (t, 2H, CH2OH, 9.6 Hz), 4.57 (br, 1H, CHCNH2), 5.09 (br, 1H, OH), 6.61 (br, 2H, NH2), 10.32 (br, 1H, NH); 13C NMR (DMSO-d6, 100 MHz): delta 44.13 (NaC2CH2), 59.28 (CH2OH), 76.52 (CHCNH2), 151.87, 157.04, 162.89. |
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