Home Chemistry Heterocyclic Building Blocks Pyrimidines Thieno[3,2-D]Pyrimidine
Reduction Reactions: Thieno[3,2-d]pyrimidine can be reduced using various reducing agents to obtain saturated or partially saturated derivatives. For example, catalytic hydrogenation or reduction with metal hydrides like lithium aluminum hydride (LiAlH4) can lead to reduced products.
Oxidation Reactions: Thieno[3,2-d]pyrimidine can be oxidized to produce various functional groups. Oxidation with reagents like potassium permanganate (KMnO4) or chromium(VI) compounds can lead to the formation of ketones, aldehydes, or other oxidized products.
Nucleophilic Substitution: The nitrogen atom in thieno[3,2-d]pyrimidine can undergo nucleophilic substitution reactions with appropriate nucleophiles. For example, primary or secondary amines can substitute the nitrogen atom to form various derivatives.
Ring Opening Reactions: Thieno[3,2-d]pyrimidine can undergo ring-opening reactions under certain conditions. This can lead to the formation of open-chain compounds with reactive functional groups.
Cyclization Reactions: Thieno[3,2-d]pyrimidine can serve as a starting material for the synthesis of other heterocyclic compounds through cyclization reactions. For instance, it can be used as a precursor in the synthesis of fused heterocycles.
Cross-Coupling Reactions: Thieno[3,2-d]pyrimidine can participate in cross-coupling reactions with various electrophiles or nucleophiles, leading to the formation of biologically active molecules or functionalized derivatives.
Functional Group Transformations: You can introduce and modify functional groups on the thieno[3,2-d]pyrimidine ring through a variety of reactions such as esterification, amidation, alkylation, and acylation.
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2-Methylthieno[3,2-d]pyrimidin-4(3H)-one
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4-Chlorothieno[3,2-d]pyrimidine-6-carbaldehyde
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Methyl thieno[3,2-d]pyrimidine-6-carboxylate
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4-Chlorothieno[3,2-d]pyrimidine-6-carboxylic acid
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Ethyl 2-chlorothieno[3,2-d]pyrimidine-4-carboxylate
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4-Chloro-2-(methylthio)thieno[3,2-d]pyrimidine
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2,4-Dichloro-7-methylthieno[3,2-d]pyrimidine
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6-(tert-Butyl)-4-chlorothieno[3,2-d]pyrimidine
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7-Bromo-2,4-dichlorothieno[3,2-d]pyrimidine
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7-Bromo-2-chlorothieno[3,2-d]pyrimidine
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2,4-Dichloro-6-methylthieno[3,2-d]pyrimidine
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