1026984-88-2

Basic information

• Product Name: [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine
• Synonyms: [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine
• CAS NO: 1026984-88-2
• Molecular Formula: C9H16N2
• Molecular Weight: 152.23674
• Mol File: 1026984-88-2.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine(CAS DataBase Reference)
• NIST Chemistry Reference: [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine(1026984-88-2)
• EPA Substance Registry System: [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine(1026984-88-2)

Safety Data

• Hazardous Substances Data: 1026984-88-2(Hazardous Substances Data)

Usage

General Description

[(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine, also known by its IUPAC name, is a chemical compound with the molecular formula C11H17N. It is a tertiary amine with a pyrrole ring and an isopropyl group. [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine is commonly used as a reagent in organic synthesis and pharmaceutical research due to its unique structure and reactivity. It can also be utilized in the production of various drug intermediates and organic compounds. Additionally, it has potential applications in the field of medicinal chemistry and drug development. Overall, [(1-methyl-1H-pyrrol-2-yl)methyl](propan-2-yl)amine is an important chemical in the field of organic chemistry and pharmaceutical research.

Upstream product

• 96-54-8 N-Methylpyrrole 

Relevant articles and documents

Piperazinylalkyl Heterocycles as Potential Antipsychotic Agents

We recently reported on a series of pyrrole Mannich bases orally active in inhibiting the conditioned avoidance response (CAR) in rats.These compounds exhibit affinity for both D2 and 5-HT1A receptors, and some are noncataleptogenic.Such a profile suggest that they may be potential antipsychotic agents which lack the propensity for causing extrapyramidal side effects and tardive dyskinesias in humans.One of these compounds, 1--1-piperazinyl>methyl>-1H-pyrrol-2-yl>methyl>-2-piperidinone (RWJ 25730, 1), was chosen for further development but found to be unstable in dilute acid.In order to improve stability, we replaced the pyrrole methylene linkage to the piperazine ring with ethylene, employed ethylene and dicarbonyl as linkers between the lactam and the pyrrole ring, placed electron-withdrawing groups on the pyrrole ring, and substituted acyclic amide for lactam.In addition, we replaced the pyrrole segment with other heterocycles including thiophene, furan, isoxazole, isoxazoline, and pyridine.Generally, replacemcent of the N-methylpyrrole segment with thiophene, furan, isoxazoline, or pyridine afforded compounds equipotent with 1 in CAR, which were more stable in dilute acid.In the case of side chain or lactam modifications, CAR activity was significantly decreased or abolished, with the exception of 6.For the most part, the modifications to 1 resulted in the decrease or loss of D2 receptor binding.However, within this series, 5-HT1A receptor binding was greatly increased, with thiophene 40 exhibiting an IC50 of 0.07 nM.The CAR activities of pyrroles 6 and 12, thiophene 40, furans 44-47, isoxazolines 49 and 50, pyridine 54 coupled with their weak or nonexistent D2 binding and strong 5-HT1A binding suggest that they may be acting via a nondopaminergic mechanism or that dopaminergic active metabolites are responsible.Pyrrole 6 and furans 44 and 47 show promise as antipsychotic agents based on their CAR activity, receptor-binding profile, and solution stability.