ChemicalBook--->CAS DataBase List--->33630-25-0

33630-25-0

33630-25-0 Structure

33630-25-0 Structure
IdentificationBack Directory
[Name]

2-Phenyl-4-aminopyrimidine
[CAS]

33630-25-0
[Synonyms]

2-Phenylpyrimidin-4-amine
2-Phenyl-4-aminopyrimidine
4-Amino-2-Phenylpyrimidine
[Molecular Formula]

C10H9N3
[MDL Number]

MFCD11043737
[MOL File]

33630-25-0.mol
[Molecular Weight]

171.2
Chemical PropertiesBack Directory
[Melting point ]

129-130 °C
[Boiling point ]

248.0±23.0 °C(Predicted)
[density ]

1.193±0.06 g/cm3(Predicted)
[storage temp. ]

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

4.71±0.10(Predicted)
[Appearance]

White to off-white Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H335-H319-H315
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
[HS Code ]

2933599590
Hazard InformationBack Directory
[Synthesis]

3-Ethoxyacrylonitrile

61310-53-0

BENZAMIDINE

618-39-3

2-Phenyl-4-aminopyrimidine

33630-25-0

General procedure for the synthesis of 2-phenylpyrimidin-4-amine from 3-ethoxyacrylonitrile and benzamidine: benzamidine (0.655 mL, 5.15 mmol) was mixed with 3-ethoxyacrylonitrile (0.500 g, 5.15 mmol) and the reaction was stirred for 3 hours at 135 °C. Upon completion of the reaction, the mixture was cooled to room temperature and stirring was continued for 16 hours. Subsequently, the solvent was removed by concentration under reduced pressure and the crude product obtained was purified by column chromatography to give 2-phenylpyrimidin-4-amine (0.545 g, 61.8% yield) as a solid. The product was analyzed by liquid chromatography-mass spectrometry (LCMS, FA mode) and showed m/z 172.4 ([M + H]+).

[References]

[1] Patent: WO2015/108861, 2015, A1. Location in patent: Paragraph 00200
[2] Patent: US2015/225422, 2015, A1. Location in patent: Paragraph 0266-0267
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