With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.191805-29-5,tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate,as a common compound, the synthetic route is as follows.
tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate from Step G (4.5 g, 17.8 mmol) was dried by evaporating with toluene (10 mL) three times in vacuo, dissolved in tetrahydrofuran (100 mL), and cooled to -78 C. To this solution was added lithium diisopropylamide mono(tetrahydrofuran) (24 mL, 36 mmol, 1.5 M in cyclohexane). The reaction mixture was stirred for 30 min at -78 C. before adding propionaldehyde (2.6 mL, 36 mmol). After 5 min, the reaction mixture was diluted with diethyl ether, poured into saturated ammonium chloride, and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to afford 6.7 g of a clear oil. The residue was purified by flash chromatography eluting with 20-30% ethyl acetate in hexanes to give the title compound (4.75 g). 1H NMR (400 MHz, CDCl3): delta 0.97 (t, 3 H), 1.33-1.37 (m, 2 H), 1.47 (s, 9 H), 1.54-1.68 (m, 5 H), 1.75-1.78 (m, 1 H), 2.07-2.13 (m, 2 H), 2.30-2.33 (m, 1 H), 2.95-3.15 (m, 2 H), 3.62-3.63 (m, 1 H), 3.84-3.94 (m, 2 H).
191805-29-5 tert-Butyl 1-oxo-8-azaspiro[4.5]decane-8-carboxylate 10848487, apiperidines compound, is more and more widely used in various.
Reference£º
Patent; Finke, Paul E.; Loebach, Jennifer L.; Parker, Kerry A.; Plummer, Christopher W.; Mills, Sander G.; US2005/70609; (2005); A1;,
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