156483-09-9

Upstream product

• 22630-09-7 trimorpholylmethane 
• 42945-85-7 2-(4-chlorophenyl)-1-(morpholin-4-yl)-ethanethione 
• 110-91-8 morpholine 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 164595-35-1 [(Z)-2-(4-Chloro-phenyl)-3-morpholin-4-yl-3-thioxo-propenylamino]-acetic acid isobutyl ester 
• 952614-01-6 2-[4-(4-chlorophenyl)-5-(morpholin-4-yl)thiophen-2-yl]-3-o-tolyl-3H-quinazolin-4-one 
• 952614-13-0 2-[4-(4-chlorophenyl)-5-(morpholin-4-yl)thiophen-2-yl]-3-p-tolyl-3H-quinazolin-4-one 
• 952613-95-5 2-[4-(4-chlorophenyl)-5-(morpholin-4-yl)thiophen-2-yl]-3-phenyl-3H-quinazolin-4-one 
• 1226763-19-4 3-(4-acetylphenyl)-2-[4-(4-chlorophenyl)-5-(morpholin-4-yl)-thiophen-2-yl]-3H-quinazolin-4-one 
• 135548-61-7 4-(4-chlorophenyl)-1-methyl-3-morpholinopyrrole-2-carboxylic acid methyl ester 
• 200862-95-9 4-(4-chlorophenyl)-1-methyl-3-morpholinopyrrole 
• 135548-91-3 4-(4-chlorophenyl)-3-morpholinopyrrole 

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

Synthesis, anticonvulsant activity, and structure-activity relationships of sodium channel blocking 3-aminopyrroles

Starting from the corresponding acetophenone and glycine derivatives, a series of new 3-aminopyrroles was synthesized in few steps. Using this procedure with hydrazine and hydroxylamine instead of the glycinates provides access to 3-aminopyrazoles and 5-a

Efficient synthesis of 3-aminothioacrylamides by iminoformylation of thioacetamides

Heating substituted thioacetamides 1 with either trismorpholinomethane or with a mixture of triethyl orthoformate and a secondary amine gives high yields of synthetically versatile 3-aminothioacrylamides 4.