59856-66-5

Basic information

• Product Name: N-(piperidin-1-yl)benzenesulfonamide
• Synonyms: N-(piperidin-1-yl)benzenesulfonamide
• CAS NO: 59856-66-5
• Molecular Weight: 240.326
• Mol File: 59856-66-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: N-(piperidin-1-yl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(piperidin-1-yl)benzenesulfonamide(59856-66-5)
• EPA Substance Registry System: N-(piperidin-1-yl)benzenesulfonamide(59856-66-5)

Safety Data

• Hazardous Substances Data: 59856-66-5(Hazardous Substances Data)

Upstream product

• 66003-76-7 Diphenyliodonium triflate 
• 2213-43-6 1-Aminopiperidine 
• 780-69-8 triethoxyphenylsilane 
• 62-53-3 aniline 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 98-09-9 benzenesulfonyl chloride 

Downstream Products

• 1582875-93-1 N-(3-methoxyphenyl)-2-[(phenylsulfonyl)(piperidin-1-yl)amino]acetamide 
• 1582875-87-3 N-(2-methoxyphenyl)-2-[(phenylsulfonyl)(piperidin-1-yl)amino]acetamide 
• 1582875-81-7 N-(2-methylphenyl)-2-[(phenylsulfonyl)(piperidin-1-yl)amino]acetamide 
• 1582875-51-1 N-(3-phenylpropyl)-N-(piperidin-1-yl)benzenesulfonamide 
• 1582875-45-3 N-(2-phenylethyl)-N-(piperidin-1-yl)benzenesulfonamide 
• 1582875-35-1 N-(4-bromobenzyl)-N-(piperidin-1-yl)benzenesulfonamide 
• 1582875-29-3 N-benzyl-N-(piperidin-1-yl)benzenesulfonamide 
• 1582875-19-1 N-allyl-N-(piperidin-1-yl)benzenesulfonamide 
• 1582875-13-5 N-ethyl-N-(piperidin-1-yl)benzenesulfonamide 
• 59856-64-3 3-Methyl-1-aethyl-5,5-pentamethylen-3,4-dihydroformazan 

Relevant articles and documents

Visible-Light Photoredox-Catalyzed Aminosulfonylation of Diaryliodonium Salts with Sulfur Dioxide and Hydrazines

A photoredox-catalyzed three-component synthesis of N-aminosulfonamides starting from diaryliodonium salts, hydrazines and sulfur dioxide is reported. This reaction proceeds under mild conditions at room temperature and is driven by visible light. A simple bisulfite salt can be used as a readily available and easy-to-handle sulfur dioxide source. Mechanistic studies support a catalytic photoredox pathway with the diaryliodonium salt as convenient source for aryl radicals. (Figure presented.).

Metal-free aminosulfonylation of aryldiazonium tetrafluoroborates with DABCO×(SO2)2 and hydrazines

The coupling of aryldiazonium tetrafluoroborates, DABCO×(SO 2)2, and hydrazines under metal-free conditions leads to the formation of aryl N-aminosulfonamides. The reaction proceeds smoothly at room temperature and shows broad functional-group tolerance. A radical process is proposed for this transformation. The coupling of aryldiazonium tetrafluoroborates, DABCO×(SO2)2, and hydrazines under metal-free conditions leads to the formation of aryl N-aminosulfonamides. The reaction proceeds under mild reaction conditions, is fast, has a broad substrate scope, and gives the products in high yiels (21 examples). A plausible mechanism that involves a radical process is also proposed. Copyright

Synthesis, spectral analysis and biological evaluation of sulfonamides bearing piperidine nucleus

In the current study, two new series of N-alkyl-N-(piperidin-1-yl) benzenesulfonamide (3a-f) and N-aryl substitued 2-[(phenylsulfonyl)- (piperidin-1-yl)amino]acetamide (5a-c) were synthesized and enzyme inhibiting activity was screened for all these chemi