Chemistry is traditionally divided into organic and inorganic chemistry. Product Details of 2213-63-0, The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent£¬Which mentioned a new discovery about 2213-63-0
Novel bridgehead nitrogen heterocyclic systems: Synthesis and antimicrobial activity of imidazo[2,1-b]-1,3,4-thiadiazolo[2,3-c]-s-triazoles, s-triazolo[3,4-b] [1,3,4]thiadiazolo[3,2-b]imidazo[4,5-b]quinoxaline and bis-(s-triazolo[3,4b][1,3,4]thiadiazolo[3,2-b] [imidazo[4,5-b]-cyclohexane]-5a, 6a-diene)
Condensation of 4-amino-5-mercapto-3-p-(t-butylphenyl)-s-triazole 1 with cyanogen bromide gives 6-amino-3-p-(tbutylphenyl)-s-triazolo[3,4-b][1,3,4]thiadiazole 2 which on condensation of with chloranil yields 3,9-di-p-(t-butylphenyl)6,14-dioxo-bis-(s-triazolo[3,4-b] [1,3,4]thiadiazolo[3,2-b]-[imidazo[4,5-b]cyclohexane]-5a,6a-diene) 3. 3-p-(t-Butylphenyl)s-triazolo[3,4-b][1,3,4]thiadiazolo[3,2-b]-imidazo [4,5-b] quinoxaline 4 is obtained by a similar condensation of 2 with 2,3-dichloroquinoxaline. The reaction of 2 with alpha-haloketones followed by bromination affords 7-aryl-3-p-(t-butylphenyl)imidazo[2,1-b]-1,3,4-thiadiazolo[2,3-c]-s-triazoles 5 and their 6-bromo analogues 6 respectively. The antibacterial and anti-fungal activities of some of the compounds have also been evaluated.
If you are interested in 2213-63-0, you can contact me at any time and look forward to more communication. Product Details of 2213-63-0
Reference£º
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N1457 | ChemSpider