30924-69-7

Upstream product

• 673-33-6 1-piperidino-1-isobutene 
• 113676-38-3 N-chloro-N'-(4-nitrobenzenesulfonyl)-benzamidine 
• 1670-14-0 benzamidine monohydrochloride 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 618-39-3 benzamidin 
• 100-52-7 benzaldehyde 
• 932-90-1 Benzaldoxime 
• 73901-01-6 p-nitrobenzenesulfonyl azide 
• 934-16-7 phenylhydroxamoyl chloride 
• 24401-44-3 β-Piperidino-α-methyl styrene 
• 28478-27-5 4-(2-phenyl-propenyl)-morpholine 

Downstream Products

• 90095-47-9 C₁₃H₉Cl₂N₃O₄S 
• 113676-40-7 N-(4-nitrobenzenesulfonyl)-N'-<(2-chloro-2-methyl-1-morpholino)-propyl>-benzamidine 
• 113676-38-3 N-chloro-N'-(4-nitrobenzenesulfonyl)-benzamidine 
• 1986-61-4 N′-(4-nitrophenyl)benzamidine 
• 90095-53-7 C₂₁H₂₅N₅O₆S₂ 
• 90095-50-4 C₁₃H₉Cl₂N₃O₄S₂ 

Relevant academic research and scientific papers

Terminal Alkyne-Assisted One-Pot Synthesis of Arylamidines: Carbon Source of the Amidine Group from Oxime Chlorides

A terminal alkyne-assisted protocol for the one-pot formation of a diverse range of arylamidines from a novel cascade reaction of in situ generated nitrile oxides, sulfonyl azides, terminal alkynes, and water by [3 + 2] cycloaddition and ring opening sequ

N-HALOAMIDINES.VI. REACTION OF N-CHLORO-N'-BENZENESULFONYLBENZAMIDINES WITH ENAMINES.

The reaction between N-chloro-N'-benzenesulfonylbenzamidines and β,β-disubstituted enamines affords N-(benzenesulfonyl)-N'--benzamidines.When both β-substituents are methyl groups the open chain adducts have been isolated and characterized, whereas, when one of the two substituents is a phenyl group, they have been characterized only by PMR because of the easy cyclization to 1-benzenesulfonyl-4,5-dihydroimidazoles.