ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

Base Information

Chemical Name:ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate
CAS No.:756486-25-6
Molecular Formula:C₂₁H₃₂N₂O₄
Molecular Weight:376.496
Hs Code.:

Synonyms:ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

Suppliers and Price of ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

There total 1 articles about ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 71.0%

: 24424-99-5
di-tert-butyl dicarbonate

: (2S,4R)-2-(ethoxycarbonyl)-1-[(1R)-phenylethyl]piperidin-4-aminium trifluoroacetate

: 756486-25-6
ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; at 20 ℃; for 5h;
DOI:10.1002/ejoc.200400045

Reference yield:

: 756486-25-6
ethyl (2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-[(1R)-phenylethyl]piperidine-2-carboxylate

: 756486-11-0
(2S,4R)-4-[(tert-butoxycarbonyl)amino]-1-(9-fluorenylmethoxycarbonyl)piperidine-2-carboxylic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 95 percent / hydrogen / Pd(OH)2/C / ethanol / 24 h / 20 °C

2: 75 percent / LiOH / methanol / 24 h / 20 °C

3: 84 percent / aq. Na₂CO₃ / acetone / 6 h / 20 °C

With lithium hydroxide; hydrogen; sodium carbonate; palladium dihydroxide; In methanol; ethanol; acetone;
DOI:10.1002/ejoc.200400045