133858-35-2

Upstream product

• 112519-62-7 4-(dimethylamino)-2-methylsulfanyl-1-phenyl-1,3-diazabuta-1,3-diene 
• 103-80-0 phenylacetyl chloride 
• 59819-37-3 4-N,N-dimethylamino-2-N-phenylamino-1-thia-3-azabutadiene 
• 112519-62-7 1-phenyl-4-dimethylamino-2-thiomethyl-1,3-diazabutadiene 

Downstream Products

• 1253786-30-9 C₁₇H₁₄N₂O₃S 

Relevant academic research and scientific papers

Concerning the nucleophilic displacement of a methylsulfanyl group on substituted pyrimidinones

The nucleophilic displacement of a methylsulfanyl group (SMe) at the C2-position on a pyrimidin-4-one scaffold was achieved after oxidation into a methylsulfonyl group (SO2Me) using dimethyldioxirane (DMDO), a powerful electrophilic oxygen atom transfer agent. The introduction of amino groups as well as formation of carbon-carbon bonds was thus demonstrated. Georg Thieme Verlag Stuttgart.

[4+2] Cycloaddition reactions of various 1,3-diaza-1.3-butadienes with ketenes

[4+2] cycloaddition reactions of 1-aryl-4-dimethylainino-1,3-diaza-1, 3-butadienes (I), 1 -aryl-4-dimethylamino-2-methylthio-1, 3-diaza-1, 3-butadienes (5), 1-aryl-4-methylthio-2-phenyl-4-sec. amino-1, 3-diaza-1, 3-butadienes (9) and 4, 4-bis(sec.amino)-1