27060-34-0

Upstream product

• 504-29-0 2-aminopyridine 
• 100-52-7 benzaldehyde 
• 103-82-2 phenylacetic acid 
• 34813-97-3 2-(formylamino)pyridine 
• 98-88-4 benzoyl chloride 
• 4589-12-2 N-(pyrid-2-yl)benzamide 

Downstream Products

• 12087-20-6 4-amino-2-phenyl-3-pyridin-2-yl-thiazolium; chloride 
• 12112-14-0 4-acetylamino-2-phenyl-3-pyridin-2-yl-thiazolium; chloride 
• 97774-21-5 bis(N-pyridin-2-yl)benzenecarbothioamide-S,N' copper(I)chloride 
• 87765-37-5 Ni(C₅H₄NNC(S)C₆H₅)2 
• 87765-39-7 Zn(C₅H₄NNC(S)C₆H₅)2 
• 87765-41-1 Hg(C₅H₄NNC(S)C₆H₅)2 
• 87765-40-0 Cd(C₅H₄NNC(S)C₆H₅)2 
• 87765-36-4 Co(C₅H₄NNC(S)C₆H₅)2 
• 87765-38-6 Cu(C₅H₄NNC(S)C₆H₅) 

Relevant academic research and scientific papers

1H AND 13C NMR STUDY OF PYRIDYLAMIDES AND THIONAMIDES

1H and 13C NMR spectra are reported for several pyridylamides and thionamides.Complete analyses of the 13C spectra have yielded the chemical shifts and the direct and long range (13C, 1H) coupling constants. 13C chemical shifts show linear relationship with charge densities computed by CNDO method.The variations in the chemical shifts are discussed.

Sulfur promoted decarboxylative thioamidation of carboxylic acids using formamides as amine proxy

An efficient decarboxylative thioamidation of arylacetic and cinnamic acids has been developed employing formamides as amine surrogate and sulfur as promoter. Thioamides with variant structural features are obtained under mild reaction conditions without the use of transition metal catalysts and oxidants.

Decarboxylative thioamidation of arylacetic and cinnamic acids: A new approach to thioamides

A new decarboxylative strategy has been developed for the synthesis of thioamides via a three-component reaction involving arylacetic or cinnamic acids, amines and elemental sulfur powder, without the need of a transition metal and an external oxidant.

Sulfated tungstate: An efficient catalyst for synthesis of thioamides via Kindler reaction

New application of sulfated tungstate, a mildly acidic solid inorganic acid, as reusable heterogeneous catalyst for efficient Kindler reaction, a three component reactions of aldehydes, amines and sulfur, for synthesis of thioamides is discussed.

N-2-PYRIDYLTHIOAMIDE DERIVATIVES AS ADDITIVES TO LUBRICANTS

The present paper deals with the synthesis of a new series of N-2-pyridylthioamide derivatives where, instead of alkyl radicals, aromatic and halogen-containing aromatic groups, having a favourable effect on the antiscuff properties of oils, are introduce