31483-56-4

Usage

Chemical Class

Pyridines

Chemical Structure

It comprises a pyridin-2-ylamine core with a 4-bromophenyl group attached at the 5th position.

Biological Activity

Potential applications in pharmaceutical research due to its structure, which suggests possible biological activity.

Applications

May be utilized in the development of new drugs or as a research tool in various scientific fields.

Variability

Precise uses and properties may vary depending on specific contexts and intended purposes.

Requirement

Further study and experimentation are necessary to fully understand its properties and potential applications.

Upstream product

• 7752-82-1 5-bromo-2-aminopyrimidine 
• 5467-74-3 4-Bromophenylboronic acid 
• 50-01-1 guanidine hydrochloride 
• 85907-67-1 2-(4-Bromophenyl)-3-(dimethylamino)-2-propenal 
• 113-00-8 guanidine nitrate 
• 1878-68-8 2-(4-bromophenyl)-acetic acid 

Downstream Products

• 942189-71-1 5-(4-piperazin-1-yl-phenyl)-pyrimidin-2-ylamine 

Relevant academic research and scientific papers

Preparation of 2,5-disubstituted pyrimidines from vinamidinium salts and synthesis of novel disulfane derivatives

Novel pyrimidine derivatives were prepared from the reaction of 2-substituted 1,3-bis(dimethylamino)-trimethinium salts with thiourea or guanidine in the presence of ethyl-diisopropylamine in ethanol at reflux, and also some 5-substituted pyrimidine-2-thi

Nitrogen-containing heterocyclic organic compounds and organic electroluminescent device (by machine translation)

The invention relates to a nitrogen-containing heterocyclic organic compounds and organic electroluminescent device, the nitrogen containing heterocyclic organic compound of the following general structure (I) shown: Wherein X is N or CH; Y is a single bo

HETEROCYCLIC COMPOUNDS AND USE THEREOF AS ERK INHIBITORS

Disclosed are the ERK inhibitors of formula 1.0: [Formula (1.0)] and the pharmaceutically acceptable salts, esters and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula 1.0.

POLYCYCLIC INDAZOLE DERIVATIVES THAT ARE ERK INHIBITORS

Disclosed are the ERK inhibitors of formula 1.0 and the pharmaceutically acceptable salts and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of formula 1.0.

PYRROLIDINE DERIVATIVES AS ERK INHIBITORS

Disclosed are the ERK inhibitors of Formula (1.0): and the pharmaceutically acceptable salts and solvates thereof. Q is a piperidine or piperazine ring that can have a bridge or a fused ring. The piperidine ring can have a double bond in the ring. All other substitutents are as defined herein. Also disclosed are methods of treating cancer using the compounds of Formula (1.0).