51627-46-4

Usage

Uses

Used in Pharmaceutical Research:
2-AZEPAN-1-YLANILINE is used as a building block for the synthesis of various pharmaceuticals and biologically active compounds, leveraging its unique structure and reactivity to contribute to the development of new therapeutic agents.
Used in Organic Synthesis:
As a versatile component in organic synthesis, 2-AZEPAN-1-YLANILINE is utilized for the preparation of novel coordination complexes, enhancing the scope of chemical reactions and expanding the range of possible products.
Used in Material Development:
2-AZEPAN-1-YLANILINE is explored for its potential in the development of new materials, where its chemical properties may contribute to the creation of innovative substances with unique properties.
Used as a Reagent in Organic Chemistry:
In the realm of organic chemistry, 2-AZEPAN-1-YLANILINE serves as a reagent, facilitating specific reactions and transformations that are otherwise challenging to achieve, thus broadening the horizons of chemical research and application.

InChI:InChI=1/C12H18N2/c13-11-7-3-4-8-12(11)14-9-5-1-2-6-10-14/h3-4,7-8H,1-2,5-6,9-10,13H2

Upstream product

• 40832-88-0 1-(2-nitrophenyl)azepane 
• 1493-27-2 ortho-nitrofluorobenzene 
• 88-73-3 2-Chloronitrobenzene 
• 111-49-9 hexamethylene imine 

Downstream Products

• 19979-46-5 7,8,9,10-tetrahydro-6H-benzo[4,5]imidazo[1,2-a]azepine 
• 1392494-25-5 N-(2-(azepan-1-yl)phenyl)-2-phenylbutanamide 
• 1392494-27-7 N-(2-(azepan-1-yl)phenyl)-2-(3-chlorophenyl)acetamide 

Relevant academic research and scientific papers

Synthesis of benzimidazoles via iridium-catalyzed acceptorless dehydrogenative coupling

Iridium-catalyzed acceptorless dehydrogenative coupling of tertiary amines and arylamines has been developed. A number of benzimidazoles were prepared in good yields. An iridium-mediated C-H activation mechanism is suggested. This finding represents a novel strategy for the synthesis of benzimidazoles.

Synthesis of benzimidazoles via iridium-catalyzed acceptorless dehydrogenative coupling

Iridium-catalyzed acceptorless dehydrogenative coupling of tertiary amines and arylamines has been developed. A number of benzimidazoles were prepared in good yields. An iridium-mediated C-H activation mechanism is suggested. This finding represents a novel strategy for the synthesis of benzimidazoles.

Synthesis of quinoxaline derivatives from substituted acetanilides through intramolecular quaternization reactions

The cyclization of 2-dialkylamino-2′-halogeno- and 2-chloro-2′-(dialkylamino)acetanilides to quinoxaline derivatives has been studied in detail. These reactions proceed, respectively, through intramolecular aromatic nucleophilic or aliphatic nucleophilic