Basic information Safety Supplier Related

2-Pyrimidinamine, 4-chloro-5-methyl- (9CI)

Basic information Safety Supplier Related

2-Pyrimidinamine, 4-chloro-5-methyl- (9CI) Basic information

Product Name:
2-Pyrimidinamine, 4-chloro-5-methyl- (9CI)
Synonyms:
  • 2-Pyrimidinamine, 4-chloro-5-methyl- (9CI)
  • 4-Chloro-5-methylpyrimidin-2-amine
  • 2-Amino-4-chloro-5-methylpyrimidine
  • 4-Chloro-5-methylpyrimidin-2-amine, 2-Amino-4-chloro-5-methyl-1,3-diazine
  • 4-Chloro-2-amino-5-methylpyrimidine
  • 4-Chloro-5-methyl-2-pyrimidinamine
  • 2-Pyrimidinamine, 4-chloro-5-methyl-
CAS:
20090-58-8
MF:
C5H6ClN3
MW:
143.57
Product Categories:
  • PYRIMIDINE
Mol File:
20090-58-8.mol
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2-Pyrimidinamine, 4-chloro-5-methyl- (9CI) Chemical Properties

Melting point:
184-185℃
Boiling point:
320.8±34.0 °C(Predicted)
Density 
1.349±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
solid
pka
3.99±0.10(Predicted)
color 
Light yellow to yellow
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Safety Information

HS Code 
2933599590
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2-Pyrimidinamine, 4-chloro-5-methyl- (9CI) Usage And Synthesis

Synthesis

15981-91-6

20090-58-8

Step b: Synthesis of 4-chloro-2-amino-5-methylpyrimidine 5-Methylisocytosine (3 g, 24.0 mmol) was mixed with phosphorus trichloride (POCl3, 20 mL) and heated to reflux for 45 minutes. Upon completion of the reaction, the excess phosphorous trichloride was removed by distillation under reduced pressure. The residue was slowly poured into ice water and the pH was subsequently adjusted to alkaline with ammonia at 10 °C. The precipitated solid was collected by filtration and recrystallized from ethanol to afford the target compound 4-chloro-2-amino-5-methylpyrimidine (1 g, 29.0% yield). 1H NMR (400 MHz, DMSO-d6) δ: 8.11 (s, 1H, pyrimidine ring H), 6.81 (br s, 2H, NH2), 2.04 (s, 3H, CH3).

References

[1] Patent: US2009/221597, 2009, A1. Location in patent: Page/Page column 41
[2] Journal of the Chemical Society, 1947, p. 41,45

2-Pyrimidinamine, 4-chloro-5-methyl- (9CI)Supplier

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