ChemicalBook--->CAS DataBase List--->1393179-35-5

1393179-35-5

1393179-35-5 Structure

1393179-35-5 Structure
IdentificationBack Directory
[Name]

2-AMino-4-chloro-pyriMidine-5-carbonitrile
[CAS]

1393179-35-5
[Synonyms]

EOS-60723
2-Amino-4-chloro-5-cyanopyrimidine
2-Amino-4-chloro-5-pyrimidinecarbonitrile
2-AMino-4-chloro-pyriMidine-5-carbonitrile
5-Pyrimidinecarbonitrile, 2-amino-4-chloro-
[Molecular Formula]

C5H3ClN4
[MDL Number]

MFCD27923125
[MOL File]

1393179-35-5.mol
[Molecular Weight]

154.56
Chemical PropertiesBack Directory
[storage temp. ]

-20°C, sealed storage, away from moisture and light
[Appearance]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

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

P280-P305+P351+P338-P310
Spectrum DetailBack Directory
[Spectrum Detail]

2-AMino-4-chloro-pyriMidine-5-carbonitrile(1393179-35-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,4-Dichloro-5-cyanopyrimidine

3177-24-0

2-AMino-4-chloro-pyriMidine-5-carbonitrile

1393179-35-5

General procedure for the synthesis of 2-amino-4-chloro-5-cyanopyrimidine from 2,4-dichloropyrimidine-5-carbonitrile: To a solution of 2,4-dichloropyrimidine-5-carbonitrile (600 mg, 3.45 mmol) in dioxane (20 mL) was added a dioxane solution of 0.5 M ammonia (20 mL, 10 mmol). The reaction mixture was stirred at room temperature for 4 hours. Upon completion of the reaction, two isomers were isolated by column chromatography using a hexane/ethyl acetate solvent mixture (ethyl acetate ratio increased from 0% to 45%). Among them, 2-amino-4-chloro-5-cyanopyrimidine (304 mg, 56% yield) was isolated as the less polar isomer. Low resolution mass spectrometry (LRMS) showed m/z of 153 (M-1).

[References]

[1] Patent: WO2012/146666, 2012, A1. Location in patent: Page/Page column 166
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