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

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

Product Name:
2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine
Synonyms:
  • deazaguanine
  • 2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine 7-Deazaguanine
  • 2-amino-1H-pyrrolo[2,3-d]pyrimidin-4-ol
  • 2-Amino-1H-pyrrolo[2,3-d]pyrimidin-4(7H)-one
  • 2-AMINO-3,7-DIHYDRO-PYRROLO[2,3-D]PYRIMIDIN-4-ONE
  • 2-AMINO-4-HYDROXY-7H-PYRROLO[2,3-DPYRIMIDINE]
  • 2-AMINO-4-HYDROXYPYRROLO-[2,3-D]PYRIMIDINE
  • 2-AMINO-7H-PYRROLO[2,3-D]PYRIMIDIN-4-OL
CAS:
7355-55-7
MF:
C6H6N4O
MW:
150.14
EINECS:
948-371-6
Product Categories:
  • PYRIMIDINE
  • AMINEPRIMARY
  • Heterocyclic Series
  • Heterocyclic Compounds
  • Bases & Related Reagents
  • Heterocycles
  • Intermediates
  • Nucleotides
Mol File:
7355-55-7.mol
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2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine Chemical Properties

Melting point:
>230°C (dec.)
Density 
1.87±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
solubility 
Soluble in N,N-Dimethylformamide, Dimethyl sulfoxide.
form 
crystalline
pka
10.83±0.20(Predicted)
color 
tan
CAS DataBase Reference
7355-55-7(CAS DataBase Reference)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
26-37-60
RIDADR 
2811
WGK Germany 
3
HazardClass 
6.1(a)
PackingGroup 
II
HS Code 
29339900

MSDS

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2-Amino-4-hydroxypyrrolo[2,3-d]pyrimidine Usage And Synthesis

Chemical Properties

Pink solid

Uses

Ethidium bromide efficiently intercalates into synthetic duplex DNAs with 7-deazaguanine in place of guanine, but shows none of the fluorescence enhancement usually observed upon intercalation. 7-Deazaadenine-duplexes show about 70% of the expected fluorescence enhancement.

Definition

ChEBI: DG is 7-deazaguanine

Synthesis

100643-27-4

2032-35-1

7355-55-7

To a suspension of bromoacetaldehyde diethyl acetal (10.4 mL, 68.98 mmol) in water (35 mL) was slowly added concentrated hydrochloric acid (1.5 mL). The reaction mixture was stirred at 90 °C for 30 min. Upon completion of the reaction, the solution was cooled to room temperature, followed by the addition of sodium acetate (6.8 g, 82.75 mmol). This mixed solution was slowly added to a suspension in water (75 mL) containing 2,4-diamino-6-hydroxypyrimidine (10.0 g, 79.29 mmol) and sodium acetate (3.5 g, 42.82 mmol). The reaction mixture was continued to be stirred at 80 °C for 2 hours. At the end of the reaction, the mixture was cooled to 0 °C and stirred for 90 min to promote crystallization. The precipitate was collected by filtration and washed sequentially with a small amount of cold water and acetone to afford the target product 2-amino-4-hydroxypyrrolo[2,3-d]pyrimidine (11.9 g, quantitative yield). The product was characterized by 1H NMR (300 MHz, DMSO-d6): δ 10.97 (s, 1H), 10.23 (s, 1H), 6.61-6.60 (m, 1H), 6.18-6.17 (m, 1H), 6.05 (s, 2H).

IC 50

DYRK1A

References

[1] Bioorganic and Medicinal Chemistry, 2018, vol. 26, # 21, p. 5596 - 5611
[2] European Journal of Organic Chemistry, 2010, # 34, p. 6517 - 6519
[3] Patent: CN103601779, 2016, B. Location in patent: Paragraph 0057; 0058; 0059
[4] Patent: CN104292117, 2016, B. Location in patent: Paragraph 0476; 0499-0501
[5] Patent: WO2014/11911, 2014, A2. Location in patent: Paragraph 00252; 00253; 00254

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