Reaction with hydrazonoyl halides. Part 32 [1]: Reaction of C-acyl-N-(3-phenyl-5-pyrazolyl)hydrazonoyl chlorides with potassium thiocyanate and synthesis of some new 2,3-dihydro-1,3,4-thiadiazoles and slenadiazoles

✍ Scribed by Abdou O. Abdelhamid; M. M. M. Sallam; S. A. Amer

• Publisher: John Wiley and Sons
• Year: 2001
• Tongue: English
• Weight: 221 KB
• Volume: 12
• Category: Article
• ISSN: 1042-7163
• DOI: 10.1002/hc.1071

✦ Synopsis

Abstract

C‐acyl‐N‐(3‐phenyl‐5‐pyrazolyl)hydrazonoyl chlorides 1a,b react with potassium thiocyanate and potassium selenocyanate to give 5‐acyl‐2,3‐dihydro‐2‐imino‐3‐(3′‐phenyl)pyrazol‐5′‐yl)‐1,3,4‐thiadiazoles 2a,b and 5‐acetyl‐2,3‐dihydro;‐2‐imino‐3‐(3′‐phenyl)pyrazol‐5′‐yl)‐1,3,4‐selenadiazole 10a,b. Also, 2‐[mercapto‐(methylthio)methylene]indan‐1,3‐dione 16 reacts with hydrazonoyl halides 15 and 22–25 to afford 2,3‐dihydro‐1,3,4‐thiadiazoles 19 and 26–29, respectively. Structures of the newly synthesized compounds are elucidated on the basis of spectral data, chemical transformations, and alternative synthesis methods. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:468–474, 2001