45715-13-7

Usage

Uses

Used in Organic Synthesis:
Methyl-(5-Methyl-pyridin-2-yl)-aMine is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure allows for versatile reactions and the formation of a wide range of products.
Used in Pharmaceutical Research:
In pharmaceutical research, Methyl-(5-Methyl-pyridin-2-yl)-aMine is employed as a key component in the development of new drugs. Its properties make it suitable for the synthesis of potential therapeutic agents.
Used in Chemical Reactions:
Methyl-(5-Methyl-pyridin-2-yl)-aMine is used as a common reagent in chemical reactions, particularly for the formation of heterocyclic compounds. Its reactivity and functional groups contribute to the synthesis of complex organic molecules.
Used in the Formation of Heterocyclic Compounds:
Methyl-(5-Methyl-pyridin-2-yl)-aMine is utilized in the synthesis of heterocyclic compounds, which are important in various fields such as pharmaceuticals, agrochemicals, and materials science. Its presence in these reactions aids in the creation of diverse and complex molecular structures.

Upstream product

• 1603-41-4 (5-methyl-pyridin-2-yl)amine 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 18368-64-4 2-chloro-5-methylpyridine 
• 74-89-5 methylamine 
• 397880-82-9 Benzotriazol-1-ylmethyl-(5-methyl-pyridin-2-yl)-amine 

Downstream Products

• 106690-38-4 2-(N-methylamino)-5-methyl-3-nitropyridine 
• 155790-13-9 N₂,5-dimethylpyridine-2,3-diamine 
• 155789-84-7 2-amino-3,6-dimethylimidazo<4,5-b>pyridine 

Relevant academic research and scientific papers

N-Methylation of Amines with Methanol Catalyzed by a Cp?Ir Complex Bearing a Functional 2,2′-Bibenzimidazole Ligand

A new type of Cp?Ir complex bearing a functional 2,2′-bibenzimidazole ligand was designed, synthesized, and found to be a highly effective and general catalyst for the N-methylation of a variety of amines with methanol in the presence of a weak base (0.3 equiv of Cs2CO3).

NOVEL COMPOUNDS FOR MODULATION OF ROR-GAMMA ACTIVITY

The present invention relates to aryl sulfones and related compounds that are modulators of ROR-gamma receptors. The invention also provides pharmaceutical compositions comprising these modulators, and methods of modulating ROR-gamma receptors using them. Also provided are methods of using aryl sulfones and related compounds as modulators of ROR-gamma to treat ROR-gamma mediated diseases

General and efficient method for direct N-monomethylation of aromatic primary amines with methanol

The direct N-monomethylation of aromatic primary amines, including arylamines, arylsulfonamides and amino-azoles, using methanol as a methylating agent has been accomplished in the presence of a [CpIrCl2]2/NaOH system. From both synthetic and environmental points of view, the reaction is highly attractive because of low catalyst loading, broad substrate scope and excellent selectivities.

2,4-DIAMINO-PYRIMIDINE DERIVATIVES

The invention concerns compounds of Formula (I), or a pharmaceutically acceptable salt thereof, where R1, Q, R3, and R4 are as defined in the description. The present invention also relates to processes for the preparation ofsuch compounds, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of EphB4 kinases.

SYNTHESIS OF THE MUTAGENIC 2-AMINO-1,6-DIMETHYLIMIDAZOPYRIDINE (1,6-DMIP) AND FIVE OF ITS ISOMERS

Synthetic routes to 2-amino-1,6-dimethylimidazopyridine and its 1,5-, 1,7-, 3,5- 3,6- and 3,7-dimethyl isomers from methyl derivatives of 3-hydroxy- or 2-amino-pyridine and 2-chloronicotinic acid are described.