887625-71-0

Upstream product

• 333-20-0 potassium thioacyanate 
• 2003-10-3 2-bromo-1-[3-(trifluoromethyl)phenyl]ethanone 
• 402-24-4 3-(trifluoromethyl)styrene 
• 1147550-11-5 ammonium thiocyanate 

Downstream Products

• 1095163-09-9 4-(3-trifluoromethyl-phenyl)-3H-thiazol-2-one 
• 1188122-51-1 2-chloro-4-(3-trifluoromethyl-phenyl)-thiazole 
• 1232234-35-3 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid 
• 1232234-36-4 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide 
• 1232234-33-1 2-amino-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide 
• 1232234-34-2 2-azido-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester 
• 1232235-18-5 2-(5-formyl-2-nitro-phenylamino)-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide 
• 1232235-17-4 2-(5-dimethoxymethyl-2-nitro-phenylamino)-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide 
• 1232234-18-2 2-[6-(4-Methyl-piperazin-1-ylmethyl)-benzoimidazol-1-yl]-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide 
• 1232235-19-6 2-[5-(4-methyl-piperazin-1-ylmethyl)-2-nitro-phenylamino]-4-(3-trifluoromethylphenyl)-thiazole-5-carboxylic acid amide 
• 74476-49-6 2-chloro-4-(3-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester 

Relevant academic research and scientific papers

Molecular oxygen induced free radical oxythiocyanation of styrenes leading to α-oxothiocyanates

A facile and efficient protocol of oxythiocyanation of styrenes with ammonium thiocyanate has been developed. The reaction proceeded at room temperature using oxygen as sole oxidant to afford the α-oxothiocyanates via radical pathway in moderate to good yields. This method is straightforward, green and cost-effective, requires no catalyst and additives.

A 2-thiocyano HYPNONE derivatives method for the preparation of

The invention discloses a method for preparing 2-sulfur cyano acetophenone derivatives. The method for preparing the 2-sulfur cyano acetophenone derivatives comprises the following steps: dissolving styrene derivatives and ammonium thiocyanate in a solvent, and reacting at 20-30 DEG C to obtain 2-sulfur cyano acetophenone derivatives. According to the method for preparing the 2-sulfur cyano acetophenone derivatives, the styrene derivatives are taken as starting materials; the raw materials are easily available and various in type; products prepared by the method have various in type, can be directly used and can also be used for other further reactions; meanwhile, the method is mild in reaction conditions and simple in reaction operation and post-processing process; an accelerant does not need to be added; the production process meets the green and chemical requirements, is relatively high in yield and is suitable for large-scale production.

Thiazolyl-Benzimidazoles

The invention is directed to compounds of formula (1) and pharmaceutically acceptable salts thereof, methods for the preparation thereof, and methods of use thereof.