Chemistry is traditionally divided into organic and inorganic chemistry. Safety of 1-Boc-4-(Aminomethyl)-4-hydroxypiperidine. The former is the study of compounds containing at least one carbon-hydrogen bonds.In a patent，Which mentioned a new discovery about 392331-66-7
The synthesis and pharmacological activity of a new series of 1-oxa-4,9-diazaspiro[5.5]undecane derivatives as potent dual ligands for the sigma-1 receptor (sigma1R) and the mu-opioid receptor (MOR) are reported. The different positions of the central scaffold, designed using a merging strategy of both target pharmacophores, were explored using a versatile synthetic approach. Phenethyl derivatives in position 9, substituted pyridyl moieties in position 4 and small alkyl groups in position 2 provided the best profiles. One of the best compounds, 15au, showed a balanced dual profile (i.e., MOR agonism and sigma antagonism) and a potent analgesic activity, comparable to the MOR agonist oxycodone in the paw pressure test in mice. Contrary to oxycodone, as expected from the addition of sigma1R antagonism, 15au showed local, peripheral activity in this test, which was reversed by the sigma1R agonist PRE-084. At equianalgesic doses, 15au showed less constipation than oxycodone, providing evidence that dual MOR agonism and sigma1R antagonism may be a useful strategy for obtaining potent and safer analgesics.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.name: 1-Boc-4-(Aminomethyl)-4-hydroxypiperidine, you can also check out more blogs about392331-66-7
Reference：
Piperidine – Wikipedia,
Piperidine | C5H18620N – PubChem