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CS-W001157 4
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7-Bromo-3-iodoimidazo[1,2-a]pyridine

  • CAS No. 1246184-55-3

  • Cat. No. CS-0056569
  • Purity≥96%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

7-Bromo-3-iodoimidazo[1,2-a]pyridine|CS-0056569

Structure of 1246184-55-3

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General Information

  • CAS No. 1246184-55-3
  • Cat. No. CS-0056569
  • Purity ≥96%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrIN₂
  • Molecular Weight 322.93
  • Synonym(s) 7-BroMo-3-iodo-iMidazo[1,2-a]pyridine
  • SMILES IC1=CN=C2C=C(Br)C=CN21

Description

7-Bromo-3-iodoimidazo[1,2-a]pyridine features a dual halogenated imidazopyridine core, enabling efficient cross-coupling reactions in medicinal chemistry. The electron-deficient aromatic system pairs well with palladium catalysts, while the bromo and iodo substituents offer orthogonal reactivity for sequential functionalization. This scaffold supports rapid diversification in target-oriented synthesis.

Application

7-Bromo-3-iodoimidazo[1,2-a]pyridine serves as a versatile bifunctional building block for the construction of imidazo[1,2-a]pyridine scaffolds in medicinal chemistry and catalytic synthesis. The bromo and iodo substituents enable sequential cross-coupling reactions with high chemoselectivity, facilitating access to complex heterocyclic architectures. Its bench-stable nature and compatibility with palladium-catalyzed coupling protocols make it well-suited for iterative functionalization in API development workflows.

Synthesis

  • Route1

    References

    • WO2010/108074 A2, ; Page/Page column 63 ; WO 2010/108074 A2

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   17.3
  • LogP   2.7014
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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