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tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate

  • CAS No. 1299607-55-8

  • Cat. No. CS-W020173
  • Purity≥95%
  • MDL No.MFCD18803503

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

tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate|CS-W020173

Structure of 1299607-55-8

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General Information

  • CAS No. 1299607-55-8
  • Cat. No. CS-W020173
  • Purity ≥95%
  • MDL No. MFCD18803503
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₂BrN₃O₂
  • Molecular Weight 298.14
  • Synonym(s) 1-Boc-5-bromo-1H-pyrazolo[3,4-b]pyridine
  • SMILES CC(C)(OC(N1C2=NC=C(Br)C=C2C=N1)=O)C

Description

tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate is a bench-stable heterocyclic building block featuring a brominated pyrazolopyridine core. This moiety integrates readily into transition-metal-catalyzed coupling reactions, enabling efficient access to functionalized N-heterocycles. The tert-butyl ester group provides enhanced solubility and stability during synthetic manipulations.

Application

tert-Butyl 5-bromo-1H-pyrazolo[3,4-b]pyridine-1-carboxylate serves as a versatile building block for the synthesis of pyrazolopyridine-based scaffolds. The bromo group enables palladium-catalyzed cross-coupling reactions, while the tert-butyl ester is readily cleaved under mild acidic conditions. This compound offers bench stability, excellent functional group tolerance, and facilitates access to biologically relevant heterocycles in medicinal chemistry and agrochemical research.

Safety Information

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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   57.01
  • LogP   2.977
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   0

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