88806-08-0

Usage

Uses

Used in Organic Synthesis:
1-(3-BROMOPROPYL)-PYRROLIDINE HYDROBROMIDE is used as a reagent in organic synthesis for its ability to facilitate specific chemical reactions, contributing to the formation of desired products in the synthesis of complex organic molecules.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 1-(3-BROMOPROPYL)-PYRROLIDINE HYDROBROMIDE is used as a research compound for exploring its potential pharmacological effects. Its study is aimed at understanding its properties and how it may contribute to the development of new drugs or therapies.
Used in Chemical Reactions:
As a reagent in chemical reactions, 1-(3-BROMOPROPYL)-PYRROLIDINE HYDROBROMIDE is used to catalyze or participate in various processes, such as the formation of new chemical bonds or the transformation of reactants into products, which is essential for advancing chemical research and development.

InChI:InChI=1/C7H14BrN.BrH/c8-4-3-7-9-5-1-2-6-9;/h1-7H2;1H

Upstream product

• 19748-66-4 3-pyrrolidin-1-yl-propan-1-ol 

Downstream Products

• 1018966-22-7 N-(3-methyl-1,2,4-thiadiazol-5-yl)-6-[(4-methyl-4H-1,2,4-triazol-3-yl)thio]-3-{[4-(3-pyrrolidin-1-ylpropoxy)phenyl]thio}pyridine-2-carboxamide 
• 1189572-62-0 C₂₆H₂₉FN₂O₃ 
• 1625669-60-4 4-(1-(3-(trifluoromethyl)phenyl)-2,5-dioxo-3-(3-(pyrrolidin-1-yl)propyl)-1,2,3,4,5,6,7,8-octahydroquinazolin-4-yl)benzonitrile 

Relevant academic research and scientific papers

2-PYRIDINECARBOXAMIDE DERIVATIVE HAVING GK-ACTIVATING EFFECT

Compounds of a formula (I) and their pharmaceutically-acceptable salts are disclosed. The compounds have glucokinase-activating effect and are therefore useful for treatment of diabetes and obesity. R1 and R2 each independently represent a lower alkyl group; X1 represent a group of a formula (II-1): wherein: R11 and R12 each independently represent a hydrogen atom or a lower alkyl group, or taken together with the nitrogen atom to which they bond, R11 and R12 may form a 4- to 7-membered nitrogen-containing aliphatic ring (one carbon atom constituting the 4- to 7-membered nitrogen-containing aliphatic ring may be replaced by an oxygen atom), or taken together with a carbon atom in (CH2)m, R11 and R12 may form a 4- to 7-membered nitrogen-containing aliphatic ring; m indicates an integer of from 1 to 3.

Electrooxidative cyclization of hydroquinolyl alcohols, hydroquinolylamines, and dimethyl aminomalonates

Several hydroquinolyl alcohols and amines were electrochemically oxidized in methanol in the presence of sodium methoxide and potassium iodide to afford the corresponding intramolecular cyclization products. Furthermore, several amino malonates were electrochemically oxidized to yield the corresponding heterocyclic compounds through an intramolecular carbon-carbon bond formation in the presence of sodium cyanide in methanol. CSIRO 2007.