30489-44-2

Usage

Uses

Used in Medicinal Chemistry:
(2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL is used as a building block for the synthesis of biologically active compounds due to its potential pharmacological properties.
Used in Pharmaceutical Industry:
(2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL is used as a precursor in the development of new drugs, leveraging its unique structure and potential interactions with biological targets for therapeutic applications.
Further research is needed to fully understand the potential applications and effects of (2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-YL)METHANOL, including its role in drug discovery and development.

InChI:InChI=1/C9H10N2O/c1-7-8(6-12)11-5-3-2-4-9(11)10-7/h2-5,12H,6H2,1H3

Upstream product

• 2549-19-1 ethyl 2-methylimidazo[1,2-a]pyridine-3-carboxylate 
• 504-29-0 2-aminopyridine 
• 30384-93-1 2-metilimidazo<1,2-a>piridin-3-carbossaldeide 

Relevant academic research and scientific papers

METHYL SULFANYL PYRMIDMES USEFUL AS ANTIINFLAMMATORIES, ANALGESICS, AND ANTIEPILEPTICS

The present invention relates to pyrimidine derivatives of Formula (Ia) and (Ib) (including tautomers, isomers, prodrugs, and pharmaceutically acceptable salts thereof). Said compounds are useful in the treatment of pain (such as neuropathic pain), inflammation, and epilepsy (by acting as anticonvulsants). Methods of medical treatment making use of said compounds, as well as additional compounds of Formula (IIa) and (IIb), are also disclosed.

BENZAZEPINE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE

The present invention provides a novel benzazepine derivative represented by formula : wherein, R1 is a 5- or 6-membered aromatic ring, R2 is lower alkyl group, etc., Y is an optionally substituted imino group, ring A and ring B are independently an optionally substituted aromatic ring, W is formula -W1-X2-W2- (W1 and W2 are independently S(O)m1 (m1 is 0, 1 or 2), etc., and X2 is an optionally substituted alkylene groupetc. ), a preparation method and use thereof.

Synthesis and biological activity of 3-substituted imidazo[1,2-a]pyridines as antiulcer agents

New imidazo[1,2-a]pyridines substituted at the 3-position have been synthesized as potential antisecretory and cytoprotective antiulcer agents. The synthetic routes began with cyclization of aminopyridines 5a,b and chloro ketones 6a,b to give imidazo[1,2-