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2-Amino-5-carboethoxy-4-hydroxypyrimidine

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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 Structure
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
pka8.26±0.50(Predicted)
color White to Orange to Green
BRN 165835
InChIKeyHRRHGLKNOJHIGY-UHFFFAOYSA-N
CAS DataBase Reference15400-53-0(CAS DataBase Reference)
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36
HS Code 2933.59.8000
MSDS Information
ProviderLanguage
ALFA English
2-Amino-5-carboethoxy-4-hydroxypyrimidine Usage And Synthesis
DefinitionChEBI: An aminopyrimidine that is 2-amino-4-hydroxypyrimidine in which the hydrogen at position 5 is substituted by an ethoxycarbonyl group.
Synthesis
carbonic acid: guanidine

124-46-9

Diethyl ethoxymethylenemalonate

87-13-8

2-AMINO-5-CARBOETHOXY-4-HYDROXYPYRIMIDINE

15400-53-0

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
Raw materialsguanidine-->Diethyl ethoxymethylenemalonate-->carbonic acid: guanidine-->Potassium hydroxide
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