98136-86-8

Usage

Uses

Used in Pharmaceutical Synthesis:
4-Amino-3,5-diiodopyridine is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications. 4-Amino-3,5-diiodopyridine's reactivity and functional groups enable the formation of new carbon-carbon and carbon-nitrogen bonds, facilitating the creation of diverse molecular structures.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-Amino-3,5-diiodopyridine serves as a crucial building block for the development of new pesticides and other agrochemicals. Its properties and reactivity contribute to the design of innovative and effective products for agricultural applications.
Used in Organic Synthesis:
4-Amino-3,5-diiodopyridine is utilized as a versatile reagent in organic synthesis. Its ability to form new bonds and participate in various chemical reactions makes it a valuable component in the synthesis of a wide range of organic compounds.
Used in Chemical Research:
As a compound with unique properties, 4-Amino-3,5-diiodopyridine is employed in chemical research to explore new reaction pathways, investigate its reactivity, and understand its potential applications in various fields. Researchers use 4-Amino-3,5-diiodopyridine to develop new synthetic methods and study its interactions with other molecules.

InChI:InChI=1/C5H4I2N2/c6-3-1-9-2-4(7)5(3)8/h1-2H,(H2,8,9)

Upstream product

• 504-24-5 4-aminopyridine 

Downstream Products

• 931104-38-0 3,5-bis-[(triphenylsilanyl)-ethynyl]-pyridin-4-ylamine 
• 6052-72-8 5,6,9,10-tetrahydro-4H,8H-pyrido[3,2,1-ij][1,6]naphthyridine 
• 931104-39-1 3,5-bis-(2-triphenylsilanyl-ethyl)-pyridin-4-ylamine 

Relevant academic research and scientific papers

Process Optimization for the Large-Scale Preparation of (2 S,3 aR,7 aS)- tert-Butyl Hexahydro-2,5-methanopyrrolo[3,2- c]pyridine-1(4 H)-carboxylate, an Intermediate for Nicotinic Acetylcholine Receptor Agonists

An optimized large-scale synthesis of (2S,3aR,7aS)-tert-butyl hexahydro-2,5-methanopyrrolo[3,2-c]pyridine-1(4H)-carboxylate (1A), an important intermediate for nicotinic acetylcholine receptor agonists, is described. The key feature of the synthesis involves three transformations in a one-pot process, including debenzylation and ring hydrogenation of two fused bicyclic rings. Multihundred gram quantities of 1A were prepared.

Palladium-catalyzed synthesis of 2,3-disubstituted 5-azaindoles via heteroannulation reaction and of 2-substituted 5-azaindoles through domino sila-Sonogashira/5-endo cyclization

A general and efficient procedure for the synthesis of 2,3-disubstituted 5-azaindoles through the palladium-catalyzed heteroannulation of 4-acetamido-3-iodopyridines and diaryl-, dialkyl-, or arylalkylalkynes is described along with a study of the reactio

TETRACYCLIC INHIBITORS OF JANUS KINASES

The present invention provides compounds that modulate the activity of Janus kinases and are useful in the treatment of diseases related to activity of Janus kinases including, for example, immune-related diseases and cancer.