The Chemistry of 2-Amino-5-bromo-3-(hydroxymethyl)pyridine: A Versatile Building Block
The utility of a chemical compound in research and industrial applications often hinges on its inherent chemical structure and the reactivity it offers. 2-Amino-5-bromo-3-(hydroxymethyl)pyridine (CAS: 335031-01-1) is a prime example of a molecule whose functional groups render it exceptionally versatile as a building block in organic synthesis, particularly within the pharmaceutical industry. Understanding its chemistry is key to unlocking its full potential.
At its core, 2-Amino-5-bromo-3-(hydroxymethyl)pyridine is a substituted pyridine. The pyridine ring, a six-membered heterocycle containing one nitrogen atom, imparts a degree of aromaticity and unique electronic properties. The substituents on this ring are what grant this specific molecule its distinct advantages. The presence of an amino group (-NH2) at the 2-position, a bromine atom (-Br) at the 5-position, and a hydroxymethyl group (-CH2OH) at the 3-position creates multiple sites for chemical transformation.
The bromine atom at the 5-position is particularly valuable for synthetic chemists. It is an excellent leaving group and a site for various palladium-catalyzed cross-coupling reactions, such as Suzuki, Heck, and Sonogashira couplings. These reactions allow for the facile introduction of carbon-carbon bonds, enabling the construction of more complex molecular frameworks. This is a critical aspect for companies looking to buy advanced intermediates for API synthesis.
The amino group at the 2-position can participate in a range of reactions, including acylation, alkylation, and diazotization, offering further avenues for functionalization. Similarly, the primary alcohol of the hydroxymethyl group can be oxidized, esterified, or etherified, providing another handle for structural modification. This trifunctional nature makes 2-Amino-5-bromo-3-(hydroxymethyl)pyridine a highly strategic molecule for drug discovery and development.
For R&D scientists and production chemists, sourcing high-purity 2-Amino-5-bromo-3-(hydroxymethyl)pyridine from reliable manufacturers and suppliers is essential. The consistent quality of this intermediate, typically offered with purities of 98% or higher, ensures predictable reaction outcomes. Whether you are exploring new synthetic routes or scaling up existing processes, the versatility of this building block, readily available from China, empowers chemists to create innovative molecules.
Perspectives & Insights
Silicon Analyst 88
“This trifunctional nature makes 2-Amino-5-bromo-3-(hydroxymethyl)pyridine a highly strategic molecule for drug discovery and development.”
Quantum Seeker Pro
“For R&D scientists and production chemists, sourcing high-purity 2-Amino-5-bromo-3-(hydroxymethyl)pyridine from reliable manufacturers and suppliers is essential.”
Bio Reader 7
“The consistent quality of this intermediate, typically offered with purities of 98% or higher, ensures predictable reaction outcomes.”