35081-79-9

Usage

InChI:InChI=1/C11H14N2OS/c15-11(13-5-7-14-8-6-13)9-10-1-3-12-4-2-10/h1-4H,5-9H2

Upstream product

• 110-91-8 morpholine 
• 100-43-6 4-vinylpyridine 
• 536-75-4 4-Ethylpyridine 
• 1122-54-9 methyl (4-pyridyl) ketone 

Downstream Products

• 28356-58-3 pyridine-4-acetic acid 
• 28487-18-5 N-[2-(4-pyridyl)ethyl]morpholine 
• 6622-91-9 2-(pyridine-4-yl)acetic acid hydrochloride 
• 73415-84-6 2-(piperidin-4-yl)acetic acid hydrochloride 
• 54401-85-3 pyridin-4-yl-acetic acid ethyl ester 
• 101793-06-0 4-(3-phenyl-2-[4]pyridyl-acryloyl)-morpholine 
• 37969-01-0 N-(3,4-dimethoxy-phenethyl)-2-pyridin-4-yl-acetamide 
• 108477-30-1 4-(3-phenyl-2-[4]pyridyl-propionyl)-morpholine 
• 109156-63-0 [4]piperidyl-acetic acid-(3,4-dimethoxy-phenethylamide) 
• 102658-91-3 [1-(3,4-dimethoxy-phenethyl)-[4]piperidyl]-acetic acid ethyl ester 
• 754124-67-9 1-[1-(3,4-dimethoxy-phenethyl)-piperidin-4-ylmethyl]-6,7-dimethoxy-3,4-dihydro-isoquinoline 
• 17289-64-4 1-[1-(3,4-dimethoxy-phenethyl)-piperidin-4-ylmethyl]-6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinoline 
• 37969-10-1 N-(3,4-dimethoxy-phenethyl)-2-[1-(3,4-dimethoxy-phenethyl)-piperidin-4-yl]-acetamide 
• 117868-22-1 1-(3,4-dimethoxy-phenethyl)-4-[(3,4-dimethoxy-phenethylcarbamoyl)-methyl]-pyridinium; iodide 

Relevant academic research and scientific papers

Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-k{cyrillic}B and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer ag

In an attempt to discover novel inhibitors of NF-κB and AP-1 mediated transcriptional activation utilizing the concept of chemical lead based medicinal chemistry and bioisosterism a series of 2-(2,3-disubstituted-thiophen-5-yl)-3H-quinazolin-4-one analogs

THIAZOLE AND THIOPHENE ANALOGUES, AND THEIR USE IN TREATING AUTOIMMUNE DISEASES AND CANCERS

Thiazole and thiophene compounds are disclosed having utility in treating inflammatory conditions, immunoinflammatory conditions, autoimmune diseases, and cancers. Methods for the synthesis of these compounds are also disclosed.

Microwave-assisted rapid hydrolysis and preparation of thioamides by Willgerodt-Kindler reaction

Aldehydes and aryl alkyl ketones were efficiently transformed to thioamides with the same number of carbon atoms via Willgerodt-Kindler reaction under microwave irradiation in solvent-free conditions. The thioamides obtained were hydrolyzed to corresponding carboxylic acids with microwave dielectric heating in one minute. Both reactions are very fast and the yields are excellent.

Microwave assisted Willgerodt-Kindler reaction of styrenes

Styrenes are efficiently transformed to thioamides via the Willgerodt- Kindler reaction under microwave irradiation.