Simple exploration of 140645-24-5

The synthetic route of 140645-24-5 has been constantly updated, and we look forward to future research findings.

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.140645-24-5,(S)-3-(Aminomethyl)-1-N-Boc-piperidine,as a common compound, the synthetic route is as follows.

Example 6: Preparation of (S)-fert-butyl 3-((2-((Z)-(2,6-dimethylphenylimino)-((?)-2-(4- (l-(4-(trifluoromethoxy)phenyl)-lH-l,2,4-triazol-3-yl)benzylidene)hydrazinyl)- methylthio)acetamido)methyl)piperidine-l-carboxylate (Compound 56C) (Synthesis Method E)To a solution of bromoacetyl bromide (26 microliters (mu), 0.299 mmol) in dichloroethane (3 mL) was added dropwise a solution of (5)-i140645-24-5

The synthetic route of 140645-24-5 has been constantly updated, and we look forward to future research findings.

Reference:
Patent; DOW AGROSCIENCES LLC; CROUSE, Gary D.; SPARKS, Thomas C.; DENT, William Hunter; MCLEOD, CaSandra Lee; CREEMER, Lawrence C.; WO2012/109125; (2012); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem