Brief introduction of 148763-41-1

The synthetic route of 148763-41-1 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.148763-41-1,Methyl N-Boc-piperidine-3-carboxylate,as a common compound, the synthetic route is as follows.

Step-1: Preparation of intermediate-43a; To a stirred solution of intermediate 42 (750 mg, 3.08 mmol) in THF (10 mL) was added a solution of lithium aluminum hydride in THF (1 M in THF, 2.16 mL) at 0 C. The reaction mass was stirred at 0 C. for 2 h. The reaction mass was quenched with sodium sulfate decahydrate. The reaction mass was filtered through a bed of celite and washed with ethyl acetate. The filtrate was evaporated to dryness. The residue was purified by flash column chromatography to afford intermediate 43a (660 mg, >99%)., 148763-41-1

The synthetic route of 148763-41-1 has been constantly updated, and we look forward to future research findings.

Reference£º
Patent; H. LUNDBECK A/S; US2011/92475; (2011); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem