156274-30-5

Upstream product

• 2365-48-2 Methyl thioglycolate 
• 1026767-91-8 2-(4-chlorophenyl)-2-cyanovinyl benzenesulfonate 
• 62538-21-0 2-(4-chloro-phenyl)-3-oxo-propionitrile 

Downstream Products

• 156274-06-5 methyl 3-(1-pyrrolyl)-4-para-chlorophenyl-2-thiophenecarboxylate 
• 1027013-41-7 4-(4-Chloro-phenyl)-3-ureido-thiophene-2-carboxylic acid ethyl ester 
• 160139-91-3 7-(4-chlorophenyl)thieno<3,2-d>pyrimidine-2,4-dione 
• 178062-60-7 3-(3-Chloro-2,2-dimethyl-propionylamino)-4-(4-chloro-phenyl)-thiophene-2-carboxylic acid methyl ester 
• 1621967-45-0 7-(4-chlorophenyl)-3-(4-methoxyphenyl)thieno[3,2-d]pyrimidin-4(3H)-one 
• 1028303-53-8 Acetic acid 2-[7-(4-chloro-phenyl)-2,4-dioxo-3,4-dihydro-2H-thieno[3,2-d]pyrimidin-1-ylmethoxy]-ethyl ester 
• 1026195-73-2 7-(4-Chloro-phenyl)-2,4-bis-trimethylsilanyloxy-thieno[3,2-d]pyrimidine 
• 156274-11-2 4-para-chlorophenyl-3-(1-pyrrolyl)-2-thiophene-N-pyrrolidinocarboxamide 

Relevant academic research and scientific papers

Expanding the scaffold for bacterial RNA polymerase inhibitors: Design, synthesis and structure-activity relationships of ureido-heterocyclic-carboxylic acids

The emergence of bacterial resistance requires the development of new antibiotics with an alternative mode of action. Based on class I, developed in our previous study, a new series of RNA polymerase (RNAP) inhibitors targeting the switch region was desig

Synthesis of thieno[3,2-d]pyrimidine-2,4-diones cyclic and acyclic nucleosides as potential anti HIV agents

Synthesis of cyclic and acyclic nucleosides was achieved by alkylation of 7-methyl or arylthieno[3,2-d]pyrimidine-2,4-diones following the Vorbruggen and Niedballa's method [1]. After a possible deprotection, potential anti HIV agents were obtained.