102254-73-9

Upstream product

• 34644-30-9 ethyl 2-(dimethylamino)-2,2-diethoxyacetate 
• 2227-79-4 benzenecarbothioamide 

Downstream Products

• 102070-55-3 bis-(4-acetyl-5-ethoxycarbonyl-2-phenypyrrol-3-yl) disulphide 
• 102070-54-2 5-ethoxycarbonyl-3-formyl-7-phenyl-2,6-dihydrothiopyrano<2,3-c>pyrrole 
• 97182-00-8 4-ethoxycarbonyl-5-formyl-2-phenyl-6H-1,3-thiazine 
• 102070-53-1 3-acetyl-2-ethoxycarbonyl-4-(3-oxobutylthio)-5-phenylpyrrole 
• 87109-03-3 5-acetyl-4-(ethoxycarbonyl)-2-phenyl-6H-1,3-thiazine 
• 134857-33-3 2-ethyl 3,4-dimethyl 5-phenyl-1H-pyrrole-2,3,4-tricarboxylate 
• 102254-85-3 3-(Bis-phenylsulfanyl-methyl)-8-oxo-6,7,7-triphenyl-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid ethyl ester 
• 102254-76-2 5-(Bis-phenylsulfanyl-methyl)-2-phenyl-6H-[1,3]thiazine-4-carboxylic acid ethyl ester 
• 95482-67-0 4-(dimethylamino)-4-(ethoxycarbonyl)-5,6-bis(methoxycarbonyl)-2-phenyl-4H-1,3-thiazine 
• 127956-59-6 4-Dimethylamino-2-phenyl-4,5-dihydro-thiazole-4-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

The Preparation and Rearrangements of 5-acyl-2-phenyl-4-substituted 6H-1,3-Thiazines. X-Ray Molecular Structure of 3-Acetyl-2-ethoxycarbonyl-4-(3-oxobutylthio)-5-phenylpyrrole

5-Acyl-2-phenyl-4-substituted 6H-1,3-thiazines are prepared by the reaction of N',N'-substituted N2-thiobenzoylformamidines with methyl vinyl ketone or acrylaldehyde.Rearrangement catalysed by base and subsequent condensation with the acrylic reagent gives substituted pyrrolyl sulphides or substituted 2,6-dihydrothiopyranopyrrole.