(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Base Information

Chemical Name:(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester
CAS No.:859855-37-1
Molecular Formula:C₂₀H₃₀N₂O₄
Molecular Weight:362.469
Hs Code.:

Synonyms:(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Suppliers and Price of (3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

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 (3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

There total 1 articles about (3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester 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: 30.0%

: 848002-72-2
(3R,4S)-1-tert-butyl 3-methyl 4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylate

: 859855-37-1
(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Guidance literature:: With sodium methylate; In methanol; at 20 - 50 ℃; for 3h;

Reference yield: 96.0%

: 859855-37-1
(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

: 859855-38-2,1620128-54-2
(3S,4S)-4-aminopiperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Guidance literature:: With ammonium formate; palladium 10% on activated carbon; In methanol; at 20 ℃; for 14h; Heating / reflux;

Reference yield:

: 859855-37-1
(3S,4S)-4-((S)-1-phenylethylamino)piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

: (3S,4S)-4-{[5-(2,4-difluorophenyl)isoxazole-3-carbonyl]amino}piperidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: palladium 10% on activated carbon; ammonium formate / methanol / 6 h / Reflux; Inert atmosphere

2: N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With palladium 10% on activated carbon; ammonium formate; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; N,N-dimethyl-formamide;