Chemistry Heterocyclic Building Blocks Pyridines thieno[2,3-c]pyridine
Ambeed provide 14 derivatives of thieno[2,3-c]pyridine.
These compounds have the same murcko framework: thieno[2,3-c]pyridine.
Electrophilic Aromatic Substitution: Thieno[2,3-c]pyridine is an aromatic compound and can undergo electrophilic aromatic substitution reactions, such as nitration, sulfonation, halogenation, and Friedel-Crafts acylation/alkylation.
Oxidation: Thieno[2,3-c]pyridine can be oxidized to form various oxidation products under appropriate conditions.
Reduction: Reduction reactions can be used to convert thieno[2,3-c]pyridine to its corresponding dihydro derivative.
Cross-Coupling Reactions: Thieno[2,3-c]pyridine can participate in cross-coupling reactions with various electrophiles or nucleophiles, such as Suzuki-Miyaura, Stille, or Heck reactions.
Cyclization: Thieno[2,3-c]pyridine can undergo intramolecular cyclization reactions to form fused or spirocycles with suitable functional groups.
Functional Group Transformations: Various reactions can be employed to modify the functional groups attached to thieno[2,3-c]pyridine, including esterification, amidation, and acylation.
Redox Reactions: Thieno[2,3-c]pyridine can be involved in redox reactions, both as an oxidant or a reductant, depending on the reaction conditions and the presence of other reagents.
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(4-Bromothieno[2,3-c]pyridin-2-yl)methanol
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Methyl 7-bromothieno[2,3-c]pyridine-2-carboxylate
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7-Bromothieno[2,3-c]pyridine-2-carboxylic acid
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Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate
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Ethyl 3-aminothieno[2,3-c]pyridine-2-carboxylate
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Methyl 4-bromothieno[2,3-c]pyridine-2-carboxylate
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Methyl 3-methylthieno[2,3-c]pyridine-2-carboxylate
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4-Fluorothieno[2,3-c]pyridine-2-carboxylic acid
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Methyl thieno[2,3-c]pyridine-3-carboxylate
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Methyl 3-aminothieno[2,3-c]pyridine-2-carboxylate