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4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE

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4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE Basic information

Product Name:
4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE
Synonyms:
  • 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE
  • 4-Amino-2-(ethylthio)-5-pyrimidinecarbonitrile
  • 5-Cyano-4-amino-2-ethylsulfanylpyrimidine
  • 5-PyriMidinecarbonitrile,4-aMino-2-(ethylthio)-
  • 4-amino-2-(ethylthio)pyrimidine-5-carbonitrile
  • 4-Amino-2-ethylsulfanyl-pyrimidine
  • 4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE ISO 9001:2015 REACH
CAS:
16462-29-6
MF:
C7H8N4S
MW:
180.23
Mol File:
16462-29-6.mol
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4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE Chemical Properties

storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
Appearance
Off-white to light yellow Solid
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4-AMINO-2-ETHYLSULFANYL-PYRIMIDINE-5-CARBONITRILE Usage And Synthesis

Synthesis

1071-37-0

123-06-8

16462-29-6

2-Ethyl-2-thiourea hydrobromide (1.52 g, 8.19 mmol) and (ethoxymethylene)malononitrile (1.0 g, 8.19 mmol) were added to a solution of N,N-diisopropylethylamine (3.57 mL, 20.05 mmol) in ethanol (20 mL). The reaction mixture was stirred at room temperature for 3.5 hours. Upon completion of the reaction, the resulting solid product was collected by filtration and washed with ethanol. Finally, the product was dried under vacuum to afford 4-amino-2-(ethylthio)-5-pyrimidine as a light yellow solid (580 mg, 39% yield).

References

[1] Patent: WO2008/133753, 2008, A2. Location in patent: Page/Page column 115
[2] Bioorganic and Medicinal Chemistry Letters, 2012, vol. 22, # 6, p. 2212 - 2215

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