Basic information Safety Supplier Related

2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile

Basic information Safety Supplier Related

2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile Basic information

Product Name:
2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile
Synonyms:
  • 2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile
  • 2-Amino-4-chloro-6-methyl-5-pyrimidinecarbonitrile
  • 5-Pyrimidinecarbonitrile, 2-amino-4-chloro-6-methyl-
CAS:
99586-66-0
MF:
C6H5ClN4
MW:
168.58
Mol File:
99586-66-0.mol
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2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
White to off-white Solid
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Safety Information

HS Code 
29335990
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2-AMino-4-chloro-6-MethylpyriMidine-5-carbonitrile Usage And Synthesis

Uses

2-Amino-4-chloro-6-methylpyrimidine-5-carbonitrile is a useful reactant for research.

Synthesis

In a 100 mL round bottom flask, 4-chloro-6-methylpyrimidin-2-amine (3 g, 21.0 mmol) was dissolved in 40 mL of glacial acetic acid and cooled in an ice bath to less than 10??C. The reaction was carried out in an ice bath. To the upper solution was added NIS (2.4 g, 10.6 mmol), the reaction was carried out for 1 hour and then NIS (2.4 g, 10.6 mmol) was added, the reaction was carried out for 1 hour and then naturally brought to room temperature for 8 hours. After the reaction was completed, the reaction solution was poured into ice water, extracted with EtOAc, the organic phase was washed with 5% Na2SO3 solution, 10% NaHCO3 solution and saturated NaCl solution, dried with anhydrous Na2SO4, filtered, and then concentrated under reduced pressure to remove the solvent, obtaining 4.9 g of solids, which was 2-amino-4-chloro-6-methylpyrimidine-5-carbonitrile, yield 87%.

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