Home Chemistry Heterocyclic Building Blocks Pyrazoles 2,3-Dihydropyrazolo[5,1-B]Oxazole
Electrophilic Substitution: If there are electron-rich regions on the molecule, it may undergo electrophilic substitution reactions with electrophilic reagents. For example, you could potentially introduce substituents on the aromatic ring of the oxazole.
Nucleophilic Addition: If there are electron-deficient regions on the molecule, it may undergo nucleophilic addition reactions with nucleophilic reagents. For instance, nucleophiles could attack the carbon atoms adjacent to the oxygen and nitrogen in the oxazole ring.
Ring Opening: The oxazole ring can potentially undergo ring-opening reactions under specific conditions. This might lead to the formation of open-chain compounds or other ring structures.
Oxidation and Reduction: Depending on the substituents and reaction conditions, you can carry out oxidation or reduction reactions on 2,3-dihydropyrazolo[5,1-b]oxazole to modify its chemical properties.
Formation of Derivatives: You can react 2,3-dihydropyrazolo[5,1-b]oxazole with various reagents to introduce functional groups, such as halogens, alkyl groups, or acyl groups, to specific positions in the molecule.
Cyclization Reactions: Depending on the reaction conditions and the presence of suitable functional groups, cyclization reactions can lead to the formation of other heterocyclic compounds or fused ring systems.
Rearrangement Reactions: Under certain conditions, rearrangement reactions can occur, leading to the formation of different isomeric products.
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(2,3-Dihydropyrazolo[5,1-b]oxazol-3-yl)methanamine hydrochloride
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2-Methyl-2,3-dihydropyrazolo[5,1-b]oxazole
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3-Methyl-2,3-dihydropyrazolo[5,1-b]oxazole
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7-Bromo-2-methyl-2,3-dihydropyrazolo[5,1-b]oxazole
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1-(7-Bromo-2,3-dihydropyrazolo[5,1-b]oxazol-3-yl)-N,N-dimethylmethanamine
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2,2-Dimethyl-2,3-dihydropyrazolo[5,1-b]oxazole
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7-Bromo-2-(methoxymethyl)-2,3-dihydropyrazolo[5,1-b]oxazole
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