Category: 177948-02-6

With the rapid development and complex challenges of chemical substances, new drug synthesis pathways are usually the most effective.177948-02-6,tert-Butyl N-[(4-hydroxypiperidin-4-yl)methyl]carbamate,as a common compound, the synthetic route is as follows.

(1) 6-Bromo-1-phenyl-1-hexanone (2.9 g) and potassium carbonate (3 g) were added to a solution of 4-hydroxy-4-tert-butoxycarbonylaminomethylpiperidine (2.5 g) in dimethylformamide (40 ml), and the mixture was stirred at 60C for 2 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform:methanol=10:1) to give 3.74 g of 4-hydroxy-1-(6-oxo-6-phenylhexyl)-4-tert-butoxycarbonylaminomethylpiperidine. 1H-NMR (CDCl3,ppm)delta:1.36-1.82(20H,m), 2.36-2.88(4H,m), 2.60-2.67(2H,m), 2.97(2H,t,J=7.3Hz), 3.14(2H,d,J=6.6Hz), 5.01(1H,br), 7.42-7.59(3H,m), 7.93-7.97(2H,m)

177948-02-6, The synthetic route of 177948-02-6 has been constantly updated, and we look forward to future research findings.

Reference：
Patent; YOSHITOMI PHARMACEUTICAL INDUSTRIES, LTD.; EP873990; (1998); A1;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem

177948-02-6, tert-Butyl N-[(4-hydroxypiperidin-4-yl)methyl]carbamate is a piperidines compound, ?involved in a variety of chemical synthesis. Rlated chemical reaction is continuously updated

1- [ (1, L-DIMETHYLETHOXYCARBONYL) AMINO]-PIPERIDINE-4-CARBOXYLIC acid (6g, 26. 16mmol, leq. ), from stepl, was dissolved in methanol (150ml) and cesium carbonate (4.26g, 13. 08mmol, 0. 5eq.) was added. The mixture was stirred at room temperature for 2h, the the solvent was removed under reduced pressure. The crude was dissolved in DMF (100ML) and benzylbromide (5.37g, 31.39mmol, 1. 2eq. ) was added dropwise. The mixture was stirred overnight at room temperature and poured in water (300ml), extracted with Ethyl Acetate (900ML) The organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure to give a white solid. Yield 95%, 7G. Analytical data: H NMR (DMSO-d6) 7.3 (5H m); 5.1 (2H, s); 3.85 (2H, d); 2.8 (2H, br); 2.65 (1H, t); 1.8 (2H, d) ; 1.4 (llH, m).

177948-02-6, 177948-02-6 tert-Butyl N-[(4-hydroxypiperidin-4-yl)methyl]carbamate 10868112, apiperidines compound, is more and more widely used in various fields.

Reference：
Patent; CEPHALON, INC.; SEDE SECONDARIA DELLA CELL THERAPEUTICS, INC.; WO2005/21558; (2005); A2;,
Piperidine – Wikipedia
Piperidine | C5H11N – PubChem