Chemistry Heterocyclic Building Blocks Imidazoles 1,1'-diphenyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
Ambeed provide 11 derivatives of 1,1'-diphenyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole.
These compounds have the same murcko framework: 1,1'-diphenyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole.
Arylation: DPh-BIM contains two phenyl groups, which are electron-rich aromatic rings. These phenyl groups can undergo various arylation reactions, such as Suzuki coupling, Stille coupling, or Heck reaction, to introduce different aryl substituents at the phenyl positions.
Halogenation: DPh-BIM can undergo halogenation reactions, such as bromination or chlorination, at the aromatic rings or other suitable positions. These reactions are often carried out using halogenating agents like N-bromosuccinimide (NBS) or chlorine gas.
N-alkylation: The nitrogen atoms in the imidazole rings can undergo N-alkylation reactions with alkyl halides or alkylating agents to introduce alkyl groups onto the imidazole nitrogen atoms.
Dehydration: In the presence of strong acids or high-temperature conditions, DPh-BIM may undergo dehydration reactions to form aromatic compounds with fewer hydrogen atoms.
Cyclization: DPh-BIM contains two imidazole rings, and under specific conditions, it may undergo intramolecular cyclization reactions to form fused-ring compounds.
Metal Complexation: The imidazole nitrogen atoms can coordinate with metal ions to form metal complexes. This property can be used in various catalytic reactions.
Cross-Coupling Reactions: DPh-BIM can participate in cross-coupling reactions with other organic compounds or reagents, leading to the formation of diverse products.
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(4S,4'S)-4,4'-Diisobutyl-1,1'-di-p-tolyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Di-tert-butyl-1,1'-di-p-tolyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisopropyl-1,1'-bis(3-isopropylphenyl)-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisopropyl-1,1'-diphenyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisopropyl-1,1'-di-m-tolyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-1,1'-Bis(3-(tert-butyl)phenyl)-4,4'-diisobutyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisopropyl-1,1'-di-p-tolyl-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisopropyl-1,1'-bis(4-methoxyphenyl)-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole
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(4S,4'S)-4,4'-Diisobutyl-1,1'-bis(3-isopropylphenyl)-4,4',5,5'-tetrahydro-1H,1'H-2,2'-biimidazole