CAS 895132-39-5

1,1-Dimethylethyl 4-(aminomethyl)-4-(2-pyridinylmethyl)-1-piperidinecarboxylate

Description:

1,1-Dimethylethyl 4-(aminomethyl)-4-(2-pyridinylmethyl)-1-piperidinecarboxylate, with CAS number 895132-39-5, is a chemical compound characterized by its complex structure, which includes a piperidine ring, a pyridine moiety, and an ester functional group. This compound typically exhibits properties associated with both amines and esters, such as potential basicity due to the presence of the amino group and the ability to participate in hydrogen bonding. The dimethyl substituents contribute to steric hindrance, which can influence its reactivity and interaction with biological targets. It may be soluble in organic solvents, and its polar functional groups can enhance solubility in polar solvents. The presence of the pyridine ring suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyridine derivatives are often associated with various biological activities. Overall, this compound's unique structural features may provide interesting avenues for research in drug design and synthesis.

Formula: C₁₇H₂₇N₃O₂

InChI: InChI=1S/C17H27N3O2/c1-16(2,3)22-15(21)20-10-7-17(13-18,8-11-20)12-14-6-4-5-9-19-14/h4-6,9H,7-8,10-13,18H2,1-3H3

InChI key: InChIKey=MYXUAWNEKBUCHC-UHFFFAOYSA-N

SMILES: C(C1(CN)CCN(C(OC(C)(C)C)=O)CC1)C2=CC=CC=N2

Synonyms:

• tert-Butyl 4-(aminomethyl)-4-[(pyridin-2-yl)methyl]piperidine-1-carboxylate
• 1,1-Dimethylethyl 4-(aminomethyl)-4-(2-pyridinylmethyl)-1-piperidinecarboxylate
• 1-Piperidinecarboxylic acid, 4-(aminomethyl)-4-(2-pyridinylmethyl)-, 1,1-dimethylethyl ester