Basic information Safety Supplier Related

5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE

Basic information Safety Supplier Related

5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE Basic information

Product Name:
5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE
Synonyms:
  • 5-METHYL-7-AZAINDOLE
  • 5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE
  • 1H-Pyrrolo[2,3-b]pyridine, 5-methyl-
CAS:
824-52-2
MF:
C8H8N2
MW:
132.16
Product Categories:
  • Aromatics
  • Heterocycles
  • Heterocycle-Pyridine series
  • Heterocycles series
Mol File:
824-52-2.mol
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5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE Chemical Properties

Melting point:
138-139 °C
Boiling point:
365.4±15.0 °C(Predicted)
Density 
1.17±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
form 
solid
pka
7.94±0.20(Predicted)
Appearance
White to light yellow Solid
InChI
InChI=1S/C8H8N2/c1-6-4-7-2-3-9-8(7)10-5-6/h2-5H,1H3,(H,9,10)
InChIKey
DJCJHFFRHKGOCQ-UHFFFAOYSA-N
SMILES
C12NC=CC1=CC(C)=CN=2
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
22-38-41
Safety Statements 
26-39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29339900
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5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE Usage And Synthesis

Chemical Properties

5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE is Light yellow solid

Uses

5-METHYL-1H-PYRROLO[2,3-B]PYRIDINE is an intermediate for preparation of pyrrolopyridine compounds as protein kinase modulators useful in treatment of diseases associated with aberrant activity of protein kinases.

Synthesis

500903-95-7

824-52-2

The general procedure for the synthesis of 5-methyl-7-azaindole from 5-methyl-3-((trimethylmethylsilyl)alkynyl)pyridin-2-amine was as follows: 5-methyl-3-((trimethylsilyl)alkynyl)pyridin-2-amine (9.8 g, 48.0 mmol) and N-methylpyrrolidinone (50 mL) were added to a dry three-necked flask. Under ice bath conditions, sodium hydride (60% dispersed in mineral oil, 2.8 g, 59 mmol) was slowly added, followed by heating the reaction mixture to 100 degrees Celsius and holding for 10 minutes. Upon completion of the reaction, the mixture was cooled to room temperature and saturated ammonium chloride solution (50 mL) was slowly added to quench the reaction. Extraction was performed with ethyl acetate (50 mL x 3) and the organic phases were combined. The organic phase was washed sequentially with water (100 mL) and saturated brine (100 mL) and then dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to dryness in a rotary evaporator to obtain the crude product. The crude product was recrystallized with ethyl acetate (10 mL) to give 5-methyl-7-azaindole (5.1 g, 38.6 mmol, 80% yield) as a white solid.

References

[1] Patent: CN107056781, 2017, A. Location in patent: Paragraph 0008
[2] Patent: WO2017/133667, 2017, A1. Location in patent: Page/Page column 120
[3] Patent: US2009/253679, 2009, A1. Location in patent: Page/Page column 41
[4] Patent: WO2008/4117, 2008, A1

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