56463-62-8

Usage

Chemical class

Pyrrole class of organic compounds

Structure

Pyrrole ring with a methyl group, an amino group, and a methoxyphenyl group attached

Potential applications

a. Development of pharmaceutical drugs
b. Chemical research and synthesis

Pharmacological properties

Not specified, but implied to be of interest for further study and exploration in the field of chemistry and pharmacology

Subject of interest

Further study and exploration in the field of chemistry and pharmacology due to its specific properties and potential applications

InChI:InChI=1/C14H16N2O2/c1-8-12(9(2)17)13(15)14(16-8)10-4-6-11(18-3)7-5-10/h4-7,16H,15H2,1-3H3

Upstream product

• 123-54-6 acetylacetone 
• 42456-26-8 2-amino-2-(4-methoxyphenyl)acetonitrile 

Relevant academic research and scientific papers

Aminopyrrole derivatives

Pharmacologically-active aminopyrrole derivatives of the formula STR1 wherein: R is selected from hydrogen, (C1-4)alkyl, benzyl and chlorobenzyl; R1 is selected from hydrogen, (C1-4)alkyl, phenyl and phenyl substituted by a radical selected from methyl, ethyl, methoxy, ethoxy, benzyloxy, fluoro, chloro and bromo; R2 and R3 individually represent hydrogen or (C1-4)alkyl or, taken together, represent an isopropylidene, a benzylidene or a chlorobenzylidene radical; R4 is selected from (C2-4)alkanoyl; carbo(C1-3)alkoxy; benzoyl, benzoyl substituted by a radical selected from chloro, methoxy or ethoxy; carbamoyl, methylcarbamoyl and phenyl carbamoyl; R5 is selected from hydrogen, (C1-4)alkyl, carbo(C1-3)alkoxy, carbomethoxymethyl, carbethoxymethyl, trifluoromethyl and carbamoyl, with the proviso that when R is hydrogen, R1 and R5 are methyl and R4 is carbethoxy, R2 and R3 cannot simultaneously represent hydrogen; And a salt thereof with a pharmaceutically acceptable acid. The compounds have anti-inflammatory and CNS-depressant utility. They are also useful as analgesics and antipyretics and display a very low degree of anti-ulcerogenic activity.