100370-83-0

Upstream product

• 13916-39-7 N-(propyl)chloroacetamide 
• 824-79-3 sodium 4-methylbenzenesulfinate 

Downstream Products

• 86562-23-4 (+/-)-3-(3-methoxyphenyl)-N-n-propylpiperidine 
• 344257-61-0 3-(4-methoxyphenyl)-1-propylpiperidine 
• 126088-53-7 3-(3-methoxyphenyl)-1-propyl-2-piperidinone 
• 19748-93-7 1-propyl-3-phenyl-piperidine 
• 62033-61-8 3-(3,4-dimethoxyphenyl)-1-propylpiperidine 
• 459453-69-1 3-phenyl-1-propylpiperidin-2-one 
• 459453-70-4 3-(4-methoxyphenyl)-1-propylpiperidin-2-one 
• 459453-71-5 3-(3,4-dimethoxyphenyl)-1-propylpiperidin-2-one 
• 459453-65-7 5-[(4-methylphenyl)sulfonyl]-3-phenyl-1-propyl-1,2,3,4-tetrahydropyridin-2-one 
• 459453-66-8 3-(3-methoxyphenyl)-5-[(4-methylphenyl)sulfonyl]-1-propyl-1,2,3,4-tetrahydropyridin-2-one 
• 459453-67-9 3-(4-methoxyphenyl)-5-[(4-methylphenyl)sulfonyl]-1-propyl-1,2,3,4-tetrahydropyridin-2-one 
• 459453-68-0 3-(3,4-dimethoxyphenyl)-5-[(4-methylphenyl)sulfonyl]-1-propyl-1,2,3,4-tetrahydropyridin-2-one 
• 459453-61-3 3-[(4-methylphenyl)sulfonyl]-5-phenyl-1-propylpiperidine-2,6-dione 

Relevant academic research and scientific papers

New synthesis of 3-aryl-N-n-propyl-piperidines

The synthesis of 3-aryl-N-n-propyl-piperidines is described in six steps starting from α-sulfonyl acetamide via the formal [3+3] cycloaddition reaction.

An efficient synthesis of N-alkyl-4-substituted 3H-pyridine-2,6-dione. Synthesis of isoguvacine and MDL-11,939

An efficient route towards the synthesis of N-alkyl-4-substituted 3H-pyridine-2,6-dione using various N-alkyl-α-sulfonylacetamides and two α,β-unsaturated esters as starting materials is described. Isoguvacine and MDL-11,939 with have potential biological activities were synthesized via this strategy.