tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

Base Information

Chemical Name:tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate
CAS No.:105259-97-0
Molecular Formula:C₂₈H₄₄N₂O₆
Molecular Weight:504.667
Hs Code.:

Synonyms:tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

Suppliers and Price of tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

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 tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

There total 5 articles about tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate 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: 75.0%

: 105259-95-8
L-alanine tert butyl ester

: 100277-54-1
ethyl (2R)-6-(1-benzyloxycarbonyl-4-piperidyl)-2-methanesulfonyloxyhexanoate

: 105259-97-0
tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

Guidance literature:: at 80 ℃; for 24h;
DOI:10.1248/cpb.42.580

Reference yield:

: 99198-61-5
ethyl 6-(1-benzyloxycarbonyl-4-piperidyl)-2-oxohexanoate

: 105259-95-8
L-alanine tert butyl ester

: 105259-96-9
tert-butyl-N-<(1R)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

: 105259-97-0
tert-butyl-N-<(1S)-5-(1-benzyloxycarbonyl-4-piperidyl)-1-ethoxycarbonylpentyl>-L-alaninate

Guidance literature:: With sodium acetate; sodium cyanoborohydride; acetic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) EtOH, 1 h, 2.) EtOH, overnight;
DOI:10.1248/cpb.42.580