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CS-W001157 4
Total: USD 88.00

3-Amino-5-bromopyridin-2(1H)-one

  • CAS No. 98786-86-8

  • Cat. No. CS-W015979
  • Purity≥97%
  • MDL No.None

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

3-Amino-5-bromopyridin-2(1H)-one|CS-W015979

Structure of 98786-86-8

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General Information

  • CAS No. 98786-86-8
  • Cat. No. CS-W015979
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₅H₅BrN₂O
  • Molecular Weight 189.01
  • Synonym(s) 3-Amino-5-bromo-2-hydroxypyridine
  • SMILES O=C1C(N)=CC(Br)=CN1

Description

3-Amino-5-bromopyridin-2(1H)-one features a brominated pyridinone core with an amino group at the 3-position, enabling direct functionalization in cross-coupling and heterocycle synthesis. The molecule exhibits enhanced solubility and stability under standard conditions, facilitating use in medicinal chemistry workflows and as a building block for bioactive compounds.

Application

3-Amino-5-bromopyridin-2(1H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the amino and bromo positions. The compound exhibits good bench stability and facilitates palladium-catalyzed cross-coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig couplings. Its dual reactive handles support efficient construction of complex heterocyclic scaffolds, particularly in kinase inhibitor and CNS-targeted drug discovery programs.

Synthesis

  • Route1

    References

    • US2005/256137 A1, ; Page/Page column 10 ;
  • Route2

    References

    • Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, , vol. 38, # 9 p. 1036 - 1040

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   58.88
  • LogP   0.7196
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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