210042-90-3

Basic information

• Product Name: C₁₅H₂₀N₈O₄S
• Synonyms: C₁₅H₂₀N₈O₄S
• CAS NO: 210042-90-3
• Molecular Weight: 408.441
• Mol File: 210042-90-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₂₀N₈O₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₂₀N₈O₄S(210042-90-3)
• EPA Substance Registry System: C₁₅H₂₀N₈O₄S(210042-90-3)

Safety Data

• Hazardous Substances Data: 210042-90-3(Hazardous Substances Data)

Upstream product

• 210042-87-8 2-(tert-Butyl-dimethyl-silanyl)-6,8-dioxo-7-phenyl-4,5,7,8-tetrahydro-6H-1,3,5a,7,8a-pentaaza-as-indacene-3-sulfonic acid dimethylamide 
• 210042-86-7 2-(tert-Butyl-dimethyl-silanyl)-6,8-dioxo-7-phenyl-5,7,8,8b-tetrahydro-6H-1,3,5a,7,8a-pentaaza-as-indacene-3-sulfonic acid dimethylamide 
• 210042-85-6 2-(tert-Butyl-dimethyl-silanyl)-5-vinyl-imidazole-1-sulfonic acid dimethylamide 
• 129378-52-5 2-tert-butyldimethylsilyl-N,N-dimethylimidazole-1-sulfonamide 
• 78162-58-0 N,N-dimethyl-1H-imidazole-1-sulfonamide 
• 210042-88-9 C₂₁H₃₄N₈O₄SSi 

Downstream Products

• 15988-11-1 4-Phenylurazole 
• 32797-32-3 dimethyl-amidosulfurous acid 
• 327-02-6 imidazo[4,5-c]pyridazine 

Relevant articles and documents

An efficient hetero Diels-Alder approach to imidazo[4,5-c]pyridazines as purine analogues

A general approach to 3-deaza-6-azapurine by a hetero Diels-Alder reaction is described. Reaction of sulfonamide protected 5-vinylimidazole with 4-phenyl-1,2,4-triazoline-3,5-dione in methanol gave the Diels-Alder adduct 8 in 85% yield. Deprotection of the resulting N-phenyltriazole was efficiently accomplished by ring opening with hydrazine followed by heating in DMSO. The completely deprotected and aromatized purine analogue 1 was obtained directly from this one-pot reaction in 48% yield.