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3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione

Base Information
  • Chemical Name:3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione
  • CAS No.:1373395-22-2
  • Molecular Formula:C26H20N2O6
  • Molecular Weight:456.455
  • Hs Code.:
3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione

Synonyms:3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione

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Chemical Property of 3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione
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Technology Process of 3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione

There total 10 articles about 3-benzyl-6,7-dihydroxy-4-(4-methoxyphenyl)-1-methyl-1H-naphtho[2,3-d]imidazole-2,5,8-trione which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 6 steps
1: manganese(IV) oxide / dichloromethane / 24 h / 20 °C
2: toluene / 24 h / 120 °C
3: sodium hypochlorite / tetrahydrofuran / 0.5 h / 0 - 20 °C
4: diisobutylaluminium hydride / hexane; dichloromethane / 4 h / -78 - 20 °C / Inert atmosphere
5: N-(tert-butyl)benzenesulfinimidoyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 0.5 h / -78 °C / Inert atmosphere
6: potassium cyanide; potassium carbonate / tetrahydrofuran; water / 0.08 h / 20 °C
With potassium cyanide; manganese(IV) oxide; sodium hypochlorite; N-(tert-butyl)benzenesulfinimidoyl chloride; diisobutylaluminium hydride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; hexane; dichloromethane; water; toluene;
DOI:10.1021/ol300704w
Guidance literature:
Multi-step reaction with 3 steps
1: diisobutylaluminium hydride / hexane; dichloromethane / 4 h / -78 - 20 °C / Inert atmosphere
2: N-(tert-butyl)benzenesulfinimidoyl chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 0.5 h / -78 °C / Inert atmosphere
3: potassium cyanide; potassium carbonate / tetrahydrofuran; water / 0.08 h / 20 °C
With potassium cyanide; N-(tert-butyl)benzenesulfinimidoyl chloride; diisobutylaluminium hydride; potassium carbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In tetrahydrofuran; hexane; dichloromethane; water;
DOI:10.1021/ol300704w
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