742085-70-7

Usage

Uses

Used in Medicinal Chemistry:
(5-Bromopyridin-2-yl)(pyrrolidin-1-yl)methanone is used as a key intermediate in the synthesis of pharmaceuticals and biologically active molecules for its ability to contribute to the development of new drugs with potential therapeutic applications.
Used in Antiviral Applications:
In the field of antiviral research, (5-Bromopyridin-2-yl)(pyrrolidin-1-yl)methanone is used as a compound with antiviral properties, potentially inhibiting the replication and spread of viruses, thereby offering a means to combat viral infections.
Used in Antibacterial Applications:
(5-Bromopyridin-2-yl)(pyrrolidin-1-yl)methanone is utilized as an antibacterial agent, leveraging its ability to target and inhibit bacterial growth, thus contributing to the development of new antibiotics to address bacterial resistance.
Used in Antifungal Applications:
(5-Bromopyridin-2-yl)(pyrrolidin-1-yl)methanone is also employed in antifungal applications, where it serves to combat fungal infections by inhibiting the growth and proliferation of fungi, providing a potential solution for treating fungal diseases.
Used in Chemical Synthesis Industry:
(5-Bromopyridin-2-yl)(pyrrolidin-1-yl)methanone is used as a versatile building block in the chemical synthesis industry, enabling the creation of a wide range of chemical substances for various applications, from pharmaceuticals to other specialty chemicals.

InChI:InChI=1/C10H11BrN2O/c11-8-3-4-9(12-7-8)10(14)13-5-1-2-6-13/h3-4,7H,1-2,5-6H2

Upstream product

• 123-75-1 pyrrolidine 
• 30766-11-1 5-bromoisonicotinic acid 
• 137178-88-2 5-bromopyridine-2-carbonyl chloride 
• 624-28-2 2,5-dibromopyridine 
• 201230-82-2 carbon monoxide 

Downstream Products

• 940314-18-1 2-(pyrrolidin-1-ylcarbonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine 

Relevant academic research and scientific papers

A thiophene and pyrimidine derivatives, its preparation process and its use in medicine

The invention discloses thiophene miazines derivates as well as a preparation method and a medical application thereof. The thiophene miazines derivates are compounds with a general formula I, a general formula II or a general formula III, wherein in the general formulae, Ar is any one of phenyl, halogen-substituted phenyl, C1-6 alkyl-substituted phenyl, biphenylyl, halogen-substituted biphenylyl, naphthyl, pyridyl, thienyl, halogen-substituted thienyl, C1-3 alkyl-substituted thienyl, furyl, halogen-substituted furyl and C1-3 alkyl-substituted furyl, A, D and E are respectively carbon atoms or nitrogen atoms but are not carbon atoms at the same time, and R is R1-NH-. The thiophene miazines derivates provided by the invention can be used for obviously restraining the activity of an EGFR (Epidermal Growth Factor Receptor) and the activity of A431 cells, are expected to be developed as a tyrosine kinase inhibitor, and are extensive in application prospect and medicinal value.

COMPOUNDS WHICH POTENTIATE AMPA RECEPTOR AND USES THEREOF IN MEDICINE

A compound of formula (I) and salts thereof are provided: wherein A is defined in the specification. Processes for preparation, pharmaceutical compositions, and uses thereof as a medicament, for example in the treatment of a disease or condition mediated by a reduction or imbalance in glutamate receptor function, such as schizophrenia or cognition impairment, are also disclosed.

Lactam compounds and methods of using the same

The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1 and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of

AMINE DERIVATIVE

The present invention provides a compound represented by the formula wherein Ar1 is a cyclic group optionally having substituent(s); R is a hydrogen atom, an optionally halogenated C1-6 alkyl, a phenyl optionally having substituent(s

SUBSTITUTED PIPERIDINES AS HISTAMINE H3 RECEPTOR LIGANDS

The present invention relates to novel piperidine ether derivatives having affinity for the histamine H3 receptor, processes for their preparation, to compositions containing them and to their use in the treatment of neurological and psychiatric disorders.