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2-Amino-4-chloropyrrolo[2,3-d]pyrimidine

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2-Amino-4-chloropyrrolo[2,3-d]pyrimidine Basic information

Product Name:
2-Amino-4-chloropyrrolo[2,3-d]pyrimidine
Synonyms:
  • 4-CHLORO-7H-PYRROLO[2,3-D]PYRIMIDIN-2-AMINE
  • 6-CHLORO-7-DEAZAGUANINE
  • 2-Amino-4-chloropyrrolo[2,3-d]pyrimidine
  • 7H-Pyrrolo[2,3-d]pyrimidin-2-amine, 4-chloro-
  • 4-CHLORO-3,7-DIHYDRO-4H-PYRROLO[2,3-D]PYRIMIDIN-2-YLAMINE
  • 4-Chloro-7H-pyrrolo[2,3-d]pyrimidin-2-ylamine
  • 2-Amino-4-Chloro-7H-pyrrolo[2,3-d]pyrimidine
  • 2-amino-6-chloro-7-deazapurine
CAS:
84955-31-7
MF:
C6H5ClN4
MW:
168.58
EINECS:
640-149-4
Product Categories:
  • CHIRAL CHEMICALS
  • Bases & Related Reagents
  • Intermediates
  • Nucleotides
Mol File:
84955-31-7.mol
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2-Amino-4-chloropyrrolo[2,3-d]pyrimidine Chemical Properties

Melting point:
215-217°C
Boiling point:
346.6±52.0 °C(Predicted)
Density 
1.82±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
DMSO (Slightly), Methanol (Slightly, Sonicated)
pka
10.68±0.20(Predicted)
form 
Powder
color 
Pale yellow to yellow
Stability:
Hygroscopic
InChI
InChI=1S/C6H5ClN4/c7-4-3-1-2-9-5(3)11-6(8)10-4/h1-2H,(H3,8,9,10,11)
InChIKey
VIVLSUIQHWGALQ-UHFFFAOYSA-N
SMILES
C1(N)=NC(Cl)=C2C=CNC2=N1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36
Safety Statements 
26
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933998090
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2-Amino-4-chloropyrrolo[2,3-d]pyrimidine Usage And Synthesis

Chemical Properties

White Crystalline Solid

Uses

6-Chloro-7-deazaguanine (cas# 84955-31-7) is a compound useful in organic synthesis.

Synthesis

7355-55-7

84955-31-7

2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine (10.0 g, 66.6 mmol) was added to 100 mL of phosphorus oxychloride (POCl3) and the reaction was carried out at reflux for 2 hours. After completion of the reaction, the solvent was removed by rotary evaporator. After the reaction mixture was cooled to room temperature, it was slowly poured into 120 mL of ice water and the solid product was collected by filtration. The filter cake was washed with ice water and the pH of the filtrate was subsequently adjusted to 2 with ammonia solution and cooled in an ice bath for 2 hours to promote precipitation. The solid product was filtered again and washed sequentially with 10 mL of ice water and 30 mL of ether, resulting in 8.7 g of 2-amino-4-chloropyrrolo[2,3-d]pyrimidine in 78% yield.

References

[1] Liebigs Annalen der Chemie, 1987, p. 15 - 19
[2] Angewandte Chemie - International Edition, 2007, vol. 46, # 13, p. 2325 - 2327
[3] Patent: CN103819523, 2016, B. Location in patent: Paragraph 0048; 0049; 0050
[4] Liebigs Annalen der Chemie, 1983, # 1, p. 137 - 146
[5] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 7, p. 2260 - 2264

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