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Energy Chemical |
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| | 2-Amino-5-carboethoxy-4-hydroxypyrimidine Basic information |
| Product Name: | 2-Amino-5-carboethoxy-4-hydroxypyrimidine | | Synonyms: | 2-Amino-4-hydroxypyrimidine-5-carboxylicacidethylester;2-Amino-5-ethoxycarbonyl-4-hydroxypyrimidine;2-Amino-5-carboethoxy-4-hydroxyprimidine;ETHYL 2-AMINO-4-HYDROXYPYRIMIDINE-5-CARBOXYLATE;LABOTEST-BB LT00455352;2-Amino-5-ethoxycarbonyl-4-hydroxypyrimidine~2-Amino-4-hydroxypyrimidine-5-carboxylic acid ethyl ester~Ethyl 2-amino-4-hydroxypyrimidine-5-carboxylate;ethyl 2-amino-1,4-dihydro-4-oxopyrimidine-5-carboxylate;2-Amino-5-carbethoxyl-4-hydroxypyrimidine | | CAS: | 15400-53-0 | | MF: | C7H9N3O3 | | MW: | 183.16 | | EINECS: | 239-418-5 | | Product Categories: | pyrimidine;Heterocycle-Pyrimidine series | | Mol File: | 15400-53-0.mol |  |
| | 2-Amino-5-carboethoxy-4-hydroxypyrimidine Chemical Properties |
| Melting point | 300°C (dec.) | | density | 1.48±0.1 g/cm3(Predicted) | | storage temp. | under inert gas (nitrogen or Argon) at 2–8 °C | | form | powder to crystal | | pka | 8.26±0.50(Predicted) | | color | White to Orange to Green | | BRN | 165835 | | InChIKey | HRRHGLKNOJHIGY-UHFFFAOYSA-N | | CAS DataBase Reference | 15400-53-0(CAS DataBase Reference) |
| Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | HS Code | 2933.59.8000 |
| Provider | Language |
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ALFA
| English |
| | 2-Amino-5-carboethoxy-4-hydroxypyrimidine Usage And Synthesis |
| Definition | ChEBI: An aminopyrimidine that is 2-amino-4-hydroxypyrimidine in which the hydrogen at position 5 is substituted by an ethoxycarbonyl group. | | Synthesis | In a 20 L three-necked flask, 1.070 Kg of potassium hydroxide (KOH) was dissolved in 10 L of distilled water and stirred until completely dissolved to form a clarified solution. Subsequently, 5 g of silica-functionalized magnetic nanoparticles (Fe3O4@SiO2) were added to the solution. Under continuous stirring, 2 Kg of guanidine carbonate was added to the above mixture to ensure its complete dissolution. The temperature of the reaction system was maintained at around 20°C. Over a period of 3 hours, 2.4 kg of diethyl ethoxymethyl malonate was slowly added dropwise while the reaction temperature was gradually increased from 20 °C to 35 °C. A yellow solid precipitated during the reaction and the reaction mixture was subsequently cooled. The Fe3O4@SiO2 particles were separated and removed using an external magnet and the particles were washed with acetone and dried. The reaction mixture was further cooled to 0-5°C and filtered to obtain a light yellow consistency, which was washed well with ice water. The crude product was recrystallized by ethanol/water solvent mixture and dried in an oven at 40°C. The dried product was divided into two parts and dissolved in 15 L of 60% water/40% ethanol mixed solvent for secondary recrystallization. The initial recrystallized solution was turbid and was clarified by steam heating for 1 hour. Subsequently, the solution began to crystallize at 39°C and was slowly cooled to room temperature. The above recrystallization process was repeated for both parts of the product and the final product was dried in a vacuum oven. Yield: 95%. | | References | [1] Asian Journal of Chemistry, 2017, vol. 29, # 10, p. 2119 - 2122 [2] Bioorganic and Medicinal Chemistry, 2007, vol. 15, # 14, p. 4841 - 4856 [3] Patent: US6194419, 2001, B1 |
| | 2-Amino-5-carboethoxy-4-hydroxypyrimidine Preparation Products And Raw materials |
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