56463-70-8

Usage

Type of compound

Heterocyclic compound

Structural components

Pyrrole ring
Amine group
Ketone functional group

Presence of substituents

4-Amino
2-methyl
5-(3-methylphenyl)

Application

Pharmaceutical research and drug development

Potential uses

Synthesis of various drugs
Building block in the preparation of new pharmaceutical compounds

Biological activities

Not specified, but implied to be significant

Role in production

Valuable intermediary in the production of medications and other biologically active substances

InChI:InChI=1/C14H16N2O/c1-8-5-4-6-11(7-8)14-13(15)12(10(3)17)9(2)16-14/h4-7,16H,15H2,1-3H3

Upstream product

• 123-54-6 acetylacetone 
• 56464-71-2 2-amino-2-(m-tolyl)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.