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2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE

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Products Intro: CAS:16462-27-4
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:2,4-Diaminopyrimidine-5-carbonitrile
CAS:16462-27-4
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-00691
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CAS:16462-27-4
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Products Intro: Product Name:2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE
CAS:16462-27-4
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Products Intro: Product Name:2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE
CAS:16462-27-4

2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE manufacturers

2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Basic information
Product Name:2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE
Synonyms:2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE;2,4-DIAMINO-5-PYRIMIDINECARBONITRILE;2,4-DIAMINO-5-CYANO-PYRIMIDINE;5-Pyrimidinecarbonitrile, 2,4-diamino- (6CI,8CI,9CI);2,4-Diaminopyrimidine-5-carbonitrile ,97%;NSC 135235;2,4-Diaminopyrimidine-5-carbonitriL;5-Pyrimidinecarbonitrile, 2,4-diamino-
CAS:16462-27-4
MF:C5H5N5
MW:135.13
EINECS:
Product Categories:Heterocycle-Pyrimidine series;Amines;Aromatics;Heterocycles;Intermediates;PYRIMIDINE
Mol File:16462-27-4.mol
2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Structure
2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Chemical Properties
Melting point 318 °C (decomp)
Boiling point 498.2±55.0 °C(Predicted)
density 1.45±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,2-8°C
solubility DMF (Slightly, Heated), DMSO (Slightly)
pka3.93±0.10(Predicted)
form Solid
color Light Yellow
Safety Information
HS Code 29335990
MSDS Information
2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Usage And Synthesis
Chemical PropertiesYellow Solid
Uses2,4-Diaminopyrimidine-5-carbonitrile is used as an intermediate for the preparation of medicines and agrochemicals (1).
UsesIntermediate for the preparation of medicines and agrochemicals.
Synthesis
Guanidine nitrate

506-93-4

Ethoxymethylenemalononitrile

123-06-8

2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE

16462-27-4

General procedure for the synthesis of 2,4-diaminopyrimidine-5-carbonitrile from guanidine nitrate and ethoxymethylenemalonononitrile: 1.22 g (10 mmol) of guanidine nitrate was dissolved in 50 mL of sodium ethanolate ethanol solution, keeping the reaction temperature at 5°C, and 1.22 g (10 mmol) of ethoxymethylenemalononitrile was added slowly dropwise, the dropwise process lasted for 8 hours. Upon completion of the reaction, the reaction was quenched by the addition of an appropriate amount of water and extracted with ethyl acetate. The organic phases were combined and washed with saturated saline, followed by concentration of the organic phase by removing the solvent by distillation under reduced pressure. Finally, the residue was purified by silica gel column chromatography with an eluent ratio of dichloromethane:methanol=1:30 (v/v) to afford the white solid product 2,4-diaminopyrimidine-5-carbonitrile (compound of formula IV) in 71% yield.

References[1] Patent: CN106938997, 2017, A. Location in patent: Paragraph 0048; 0058-0059
[2] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 9, p. 3187 - 3197
2,4-DIAMINOPYRIMIDINE-5-CARBONITRILE Preparation Products And Raw materials
Raw materialsGuanidine hydrochloride-->2,4-Diamino-5-pyrimidinemethanol-->2,6-DIETHYLPHENOL-->Ethoxymethylenemalononitrile-->Ethanol
Preparation Products2,4-Diamino-5-pyrimidinemethanol
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