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2-Amino-5-hydroxypyrimidine

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2-Amino-5-hydroxypyrimidine manufacturers

2-Amino-5-hydroxypyrimidine Basic information
Product Name:2-Amino-5-hydroxypyrimidine
Synonyms:2-Amido-5-hydroxyprimidine;2-Aminopyrimidin-5-ol, 5-Hydroxypyrimidin-2-amine;2-AMino-5-hydroxypyriMidi...;2-Amino-pyrimidin-5-ol;5-Pyrimidinol, 2-amino- (9CI);2-Amino-5-pyrimidinol;2-Amino-5-hydroxypyrimidine;5-Pyrimidinol, 2-amino-
CAS:143489-45-6
MF:C4H5N3O
MW:111.1
EINECS:
Product Categories:Heterocycle-Pyrimidine series;Heterocyclic Compounds;Pyrimidines;Bases & Related Reagents;Heterocycles;Nucleotides;PYRIMIDINE;Heterocyclic Series
Mol File:143489-45-6.mol
2-Amino-5-hydroxypyrimidine Structure
2-Amino-5-hydroxypyrimidine Chemical Properties
Melting point >170°C (dec.)
Boiling point 393.6±34.0 °C(Predicted)
density 1.450±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility DMSO (Slightly), Methanol (Slightly, Sonicated)
pka3.95±0.23(Predicted)
form Powder or Crystalline Powder
color White to yellow
CAS DataBase Reference143489-45-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36-36/37/39
HazardClass IRRITANT
HS Code 25010019
MSDS Information
2-Amino-5-hydroxypyrimidine Usage And Synthesis
Chemical PropertiesWhite Solid
Uses2-Aminopyrimidin-5-ol is an endogenous metabolite.
DefinitionChEBI: 2-Amino-5-hydroxypyrimidine is a hydroxypyrimidine.
Synthesis
2-AMINO-5-METHOXYPYRIMIDINE

13418-77-4

2-Amino-5-hydroxypyrimidine

143489-45-6

Boron tribromide (2.6 mL, 50 mmol) was slowly added dropwise to a benzene solution (60 mL) containing 5-methoxy-2-aminopyrimidine (1.25 g, 10 mmol) under argon protection. The reaction mixture was stirred under reflux conditions for 6 hours. After completion of the reaction, the mixture was allowed to stand at room temperature overnight. Subsequently, the solvent was removed by rotary evaporator and the residue was carefully treated with ice-cold deionized water (10 mL). The solution pH was adjusted to 6-7 using 6N hydrochloric acid and subsequently extracted with ethyl acetate. The organic phase was washed with saturated saline, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated to give a yellow solid, which was purified by column chromatography (eluent ratio of 20:1 dichloromethane to methanol) to give 840 mg (75% yield) of 2-aminopyrimidin-5-ol as a white solid. The structure of the product was confirmed by 1H-NMR and electron bombardment mass spectrometry (EI-MS).1H NMR (DMSO-d6) δ 8.90 (s, 1H), 7.86 (s, 2H), 5.91 (s, 2H); EI-MS (m/z) 111 (M+).

References[1] European Journal of Medicinal Chemistry, 1992, vol. 27, # 3, p. 207 - 217
[2] Patent: US2009/105269, 2009, A1. Location in patent: Page/Page column 10
[3] Journal of Medicinal Chemistry, 2010, vol. 53, # 3, p. 1117 - 1127
2-Amino-5-hydroxypyrimidine Preparation Products And Raw materials
Raw materials2-Amino-5-methoxypyrimidine-->Benzene-->Boron tribromide
Tag:2-Amino-5-hydroxypyrimidine(143489-45-6) Related Product Information
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