The Chemical Properties and Synthesis of Tert-butyl 4-aminopiperidine-1-carboxylate Hydrochloride
At NINGBO INNO PHARMCHEM CO.,LTD., we are dedicated to providing detailed insights into the chemical compounds we supply, including tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride. This compound, identified by CAS number 189819-75-8, is a valuable organic chemical intermediate with a specific molecular formula of C10H21ClN2O2 and a molecular weight of approximately 236.74 g/mol. Understanding its chemical properties is crucial for its effective application in synthesis.
Tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride typically presents as a white powder, indicating its solid state under standard conditions. Its structure features a piperidine ring, a tert-butyl carbamate (Boc) protecting group, and an amine functionality, all stabilized as a hydrochloride salt. This unique combination of functional groups makes it a versatile building block for a wide range of organic transformations. The Boc group offers protection to the piperidine nitrogen, allowing selective reactions at the amine group, a common strategy in complex organic synthesis and the tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride synthesis.
The synthesis of tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride involves established organic chemistry procedures. While specific proprietary methods may vary, the process generally entails functionalizing a piperidine precursor and then introducing the Boc protecting group, followed by salt formation. NINGBO INNO PHARMCHEM CO.,LTD. focuses on optimizing these synthesis routes to achieve high yields and purity, ensuring that our clients, who may be looking for tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride with high purity 4-amino-1-boc-piperidine hydrochloride, receive a product that meets their exact specifications.
As a key pharmaceutical intermediate, the compound's reactivity and stability are critical. The presence of the amine group allows for nucleophilic substitution and amide formation, while the ester linkage within the Boc group can be cleaved under specific conditions. These characteristics make it an ideal starting material for constructing more complex molecules, including those found in pharmaceutical APIs. The meticulous control over synthesis conditions by NINGBO INNO PHARMCHEM CO.,LTD. ensures that these reactive sites are well-defined and accessible for subsequent reactions.
In essence, the chemical properties of tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride, coupled with efficient synthesis methodologies, position it as a vital component in the chemical industry. NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing comprehensive product information and high-quality materials, including this essential pharmaceutical building block, to support our clients' ongoing research and development efforts.
Perspectives & Insights
Agile Reader One
“focuses on optimizing these synthesis routes to achieve high yields and purity, ensuring that our clients, who may be looking for tert-butyl 4-aminopiperidine-1-carboxylate hydrochloride with high purity 4-amino-1-boc-piperidine hydrochloride, receive a product that meets their exact specifications.”
Logic Vision Labs
“As a key pharmaceutical intermediate, the compound's reactivity and stability are critical.”
Molecule Origin 88
“The presence of the amine group allows for nucleophilic substitution and amide formation, while the ester linkage within the Boc group can be cleaved under specific conditions.”