ChemicalBook--->CAS DataBase List--->4922-68-3

4922-68-3

4922-68-3 Structure

4922-68-3 Structure
IdentificationBack Directory
[Name]

3-Bromo-[1,2,4]triazolo[4,3-a]pyridine
[CAS]

4922-68-3
[Synonyms]

Ponatinib Impurity 9
s-Triazolo[4,3-a]pyridine, 3-bromo-
3-bromo-[1,2,4]triazolo[4,3-a]pyridine
1,2,4-TRIAZOLO[4,3-A]PYRIDINE, 3-BROMO-
[Molecular Formula]

C6H4BrN3
[MDL Number]

MFCD11111699
[MOL File]

4922-68-3.mol
[Molecular Weight]

198.02
Chemical PropertiesBack Directory
[Melting point ]

165-167 °C
[density ]

1.89±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[pka]

0.97±0.50(Predicted)
[Appearance]

Light brown to brown Solid
[InChI]

InChI=1S/C6H4BrN3/c7-6-9-8-5-3-1-2-4-10(5)6/h1-4H
[InChIKey]

BOKHADJFZUWNSH-UHFFFAOYSA-N
[SMILES]

C12=NN=C(Br)N1C=CC=C2
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H310-H302-H315-H319
[Precautionary statements ]

P501-P270-P262-P264-P280-P337+P313-P305+P351+P338-P361+P364-P332+P313-P301+P312+P330-P302+P352+P310-P405
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

3-Bromo-[1,2,4]triazolo[4,3-a]pyridine is an intermediate used to prepare bi-aryl amines as mGluR5 modulators for treating gastrointestinal, urinary tract, and nervous system disorders.
[Synthesis]

1,7,8-triazabicyclo[4.3.0]nona-2,4,6,8-tetraene

274-80-6

3-Bromo-[1,2,4]triazolo[4,3-a]pyridine

4922-68-3

General procedure for the synthesis of 3-bromo-[1,2,4]triazolo[4,3-a]pyridine from [1,2,4]triazolo[4,3-a]pyridine: [1,2,4]triazolo[4,3-a]pyridine (1.26 g) and N-bromosuccinimide (NBS, 1.98 g) were dissolved in chloroform, and the reaction was carried out at reflux for 5 h followed by a 14-h stand at room temperature. Upon completion of the reaction, saturated aqueous potassium carbonate (200 mL) and potassium hydroxide (20 g) were added to the mixture, and the organic layer was separated after sufficient shaking. The aqueous layer was extracted twice with dichloromethane (DCM). All organic layers were combined and dried over anhydrous sodium sulfate (Na2SO4) followed by evaporation of the solvent under vacuum to afford the target product 3-bromo-[1,2,4]triazolo[4,3-a]pyridine in 60% yield.

[References]

[1] Patent: EP2743266, 2014, A2. Location in patent: Page/Page column
Spectrum DetailBack Directory
[Spectrum Detail]

3-Bromo-[1,2,4]triazolo[4,3-a]pyridine(4922-68-3)1HNMR
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