7120-14-1

Usage

InChI:InChI=1/C11H7N3O2S/c15-14(16)9-3-1-8(2-4-9)10-7-13-5-6-17-11(13)12-10/h1-7H

Upstream product

• 96-50-4 2-thiazolylamine 
• 99-81-0 4-Nitrophenacyl bromide 
• 99973-22-5 6-(4-nitro-phenyl)-2,3-dihydro-imidazo[2,1-b]thiazol-3-ol 
• 7008-63-1 6-phenylimidazo[2,1-b]thiazole 
• 6857-35-8 4-(4-nitro-phenyl)-1,3-dihydro-imidazole-2-thione 
• 70-11-1 α-bromoacetophenone 
• 100-19-6 (4-nitrophenyl)ethanone 
• 56177-37-8 1-(4-nitrophenyl)-2-(p-tolylsulfonyloxy)ethanone 

Downstream Products

• 183668-02-2 6-(4-aminophenyl)imidazo<2,1-b>thiazole 
• 66517-21-3 5-bromo-6-p-nitrophenylimidazo<2,1-b>thiazole 
• 16311-38-9 5-nitro-6-(4-nitro-phenyl)-imidazo[2,1-b]thiazole 
• 134670-32-9 C₁₁H₆⁽²⁾HN₃O₂S 
• 118001-65-3 acetic acid-(4-imidazo[2,1-b]thiazol-6-yl-anilide) 

Relevant academic research and scientific papers

Hypervalent iodine(iii) sulfonate mediated synthesis of 6-arylimidazo[2,1-b]thiazoles in liquid PEG-400

PEG-400[poly(ethylene glycol-400)] is used as reaction medium in the one-pot synthesis of 6-arylimidazo[ 2,1-b]thiazoles by reaction with aryl ketones, hypervalent iodine(III) sulfonate and 2-aminothiazole. Significant rate enhancements and improved yield

Hypervalent iodine in the synthesis of bridgehead heterocycles: A facile route to the synthesis of 6-arylimidazo[2,1-b]thiazoles using [hydroxy(tosyloxy)iodo]benzene

α-Tosyloxyketones (2), readily accessible through hypervalent iodine oxidation of enolizable ketones (1) using [hydroxy(tosyloxy)iodo]benzene (HTIB) in acetonitrile, exclusively generates the 6-arylimidazo[2,1-b]thiazoles (4) on treatment with commerciall

Substituted imidazo[2,1-b]thiazoles from 2-aminothiazoles and α-bromo ketones: Efficient preparation and proof of structure

The salts formed from α-aminothiazoles and α-bromo ketones (RCOCH2Br) have been basified, and the products converted into amides. Examination of the amides established that they are 2-acylimino-2,3- dihydrothiazoles rather than 2-acylaminothiaz