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AA20306

1150617-54-1 | 6-Bromo-1H-pyrazolo[4,3-b]pyridine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $8.00 $5.00 -   +
250mg 97% in stock $9.00 $6.00 -   +
1g 97% in stock $18.00 $12.00 -   +
2.5g 97% in stock $42.00 $29.00 -   +
5g 97% in stock $48.00 $33.00 -   +
10g 97% in stock $95.00 $66.00 -   +
25g 97% in stock $236.00 $165.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA20306
Chemical Name: 6-Bromo-1H-pyrazolo[4,3-b]pyridine
CAS Number: 1150617-54-1
Molecular Formula: C6H4BrN3
Molecular Weight: 198.0201
MDL Number: MFCD12024534
SMILES: Brc1cc2[nH]ncc2nc1

 

Computed Properties
Complexity: 130  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • To synthesize 6-Bromo-1H-pyrazolo[4,3-b]pyridine, start with the appropriate pyrazolopyridine precursor. The upstream synthesis route involves the following steps:
    
    1. Synthesis of Pyrazolopyridine Core:
       - Condense an aminopyridine with a suitable β-diketone under acidic conditions to obtain the pyrazolopyridine core.
    
    2. Bromination:
       - Subject the pyrazolopyridine core to bromination using a brominating agent such as N-Bromosuccinimide (NBS) in the presence of a solvent like dichloromethane (DCM) at 0°C to room temperature.
       - Ensure the reaction is carried out under anhydrous conditions to prevent side reactions with water. 
    
    3. Purification:
       - After bromination, purify the product via column chromatography or recrystallization to obtain the desired 6-Bromo-1H-pyrazolo[4,3-b]pyridine with high purity.
    
    Further specifics of the reaction conditions would need to be optimized based on the particular starting materials and desired scale of the synthesis.
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