883231-14-9

Usage

Uses

Used in Pharmaceutical Development:
(6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)boronic acid is used as a building block for the development of pharmaceuticals due to its unique structure and reactivity. Its potential applications in the creation of new drugs are being explored.
Used in Organic Synthesis:
In the field of organic synthesis, (6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)boronic acid is used as a reagent, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are crucial for forming carbon-carbon bonds, which are essential in constructing complex organic molecules.
Used in Material Science:
(6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)boronic acid may also find applications in material science, where its unique structure could contribute to the development of novel organic materials with specific properties.
Safety and Precautions:
As with any chemical compound, it is essential to handle (6-(2-methyl-2H-tetrazol-5-yl)pyridin-3-yl)boronic acid with care and follow proper safety protocols to ensure the safety of those working with it and to maintain its effectiveness for intended applications.

Upstream product

• 5419-55-6 Triisopropyl borate 
• 380380-64-3 5-bromo-2-(2-methyl-2H-tetrazol-5-yl)pyridine 
• 380380-63-2 2-(1-methyl-1,2,3,4-tetrazol-5-yl)-5-bromopyridine 

Relevant academic research and scientific papers

Preparation method of oxazolidinone antibiotic intermediate

The invention provides a preparation method of a tedizolid phosphate intermediate compound 3-fluoro-4-(6-(2-methyltetrazole-5-yl)pyridine-3-yl)phenyl benzyl carbamate. The method comprises the following steps: carrying out a reaction on 5-bromo-2-(2-methyltetrazole-5-yl)pyridine as a raw material and triisopropyl borate under the action of n-butyllithium to prepare a boric acid intermediate, coupling the boric acid intermediate and 1,2-difluoro-4-nitrobenzene, and finally performing nitro reduction and amidation to obtain the required target product. Compared with the method in the prior art,the preparation method disclosed by the invention has the advantages of easily available raw materials, simple process, economy, environmental protection and suitability for industrial production.

A oxazolidinone compounds of preparation method (by machine translation)

The invention provides a oxazolidinone compounds of the preparation method. Specifically provides the type 1 compound preparation method. The formula 1 compound preparation method comprises, formula 2 N - methyl - D - grape amine compound in the presence of a catalytic reduction, direct formula 1 compound. The present invention provides a preparation has simplified the reaction step, shorten the reaction route, can make the final yield of the product is higher, and, better purity. (by machine translation)

OXAZOLIDINONE DERIVATIVES AS ANTIMICROBIALS

The present invention relates to certain substituted phenyl oxazolidinones and to processes for the synthesis of the same. This invention also relates to pharmaceutical compositions containing the compounds of the present invention as antimicrobials. The compounds are useful antimicrobial agents, effective against a number of human and veterinary pathogens, including gram-positive aerobic bacteria, for example, multiple-resistant staphylococci, streptococci and enterococci as well as anaerobic organisms, for example, Bacterioides spp. and Clostridia spp. species, and acid fast organisms, for example, Mycobacterium tuberculosis, Mycobacterium avium and Mycobacterium spp.