ChemicalBook--->CAS DataBase List--->22715-27-1

22715-27-1

22715-27-1 Structure

22715-27-1 Structure
IdentificationBack Directory
[Name]

2,5-Diaminopyrimidine
[CAS]

22715-27-1
[Synonyms]

2,5-DIAMINOPYRIMIDINE
2,5-Pyrimidinediamine
2,5-Diaminepyrimidine
pyrimidine-2,5-diamine
Pyrimidine, 2,5-diamino-
2,5-Pyrimidinediamine (9CI)
(2-aminopyrimidin-5-yl)amine
2,5-Diaminopyrimidine ISO 9001:2015 REACH
[Molecular Formula]

C4H6N4
[MDL Number]

MFCD00129726
[MOL File]

22715-27-1.mol
[Molecular Weight]

110.12
Chemical PropertiesBack Directory
[Melting point ]

200 °C
[Boiling point ]

401.7±37.0 °C(Predicted)
[density ]

1.368±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[pka]

4.83±0.10(Predicted)
[Appearance]

Yellow to brown Solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

2-Amino-5-nitropyrimidine
Spectrum DetailBack Directory
[Spectrum Detail]

2,5-Diaminopyrimidine(22715-27-1)MS
2,5-Diaminopyrimidine(22715-27-1)1HNMR
2,5-Diaminopyrimidine(22715-27-1)IR1
2,5-Diaminopyrimidine(22715-27-1)IR2
Hazard InformationBack Directory
[Synthesis]

2-Amino-5-nitropyrimidine

3073-77-6

2,5-Diaminopyrimidine

22715-27-1

Synthesis of I-5: To a 1L round bottom flask was added 5-nitropyrimidin-2-amine (30 g, 214.13 mmol, 1.00 eq.), methanol (400 mL) and palladium carbon (12 g). The reaction mixture was stirred overnight at room temperature in a hydrogen atmosphere. Upon completion of the reaction, the solid catalyst was removed by filtration. The filtrate was concentrated under reduced pressure to afford pyrimidine-2,5-diamine (20 g, 85% yield) as a light brown solid.

[References]

[1] Patent: US7235559, 2007, B1
[2] Patent: US2014/275119, 2014, A1. Location in patent: Paragraph 0416
[3] Journal of the American Chemical Society, 1942, vol. 64, p. 2340
[4] Journal of Medicinal Chemistry, 2008, vol. 51, # 6, p. 1681 - 1694
[5] Patent: WO2010/111483, 2010, A1. Location in patent: Page/Page column 90
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