(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Base Information

Chemical Name:(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester
CAS No.:1147551-56-1
Molecular Formula:C₃₅H₃₆N₄O₅
Molecular Weight:592.695
Hs Code.:

Synonyms:(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Suppliers and Price of (3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl 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,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

There total 4 articles about (3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl 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:

: C₃₆H₃₉NO₈S

: 1147551-56-1
(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Guidance literature:: With sodium azide; In N,N-dimethyl-formamide; at 90 ℃; for 60h;
DOI:10.1021/ja809776r

Reference yield:

: 6-azido-2,3,4-tri-O-benzyl-6-deoxy-α,β-D-glucopyranose

: 1147551-56-1
(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: triphenylphosphine polymer bound / tetrahydrofuran / 40 °C

1.2: 14 h / 20 °C

1.3: 0 - 20 °C

2.1: dmap; pyridine / 0 - 20 °C / Inert atmosphere

3.1: sodium azide / N,N-dimethyl-formamide / 96 h / 90 °C

With pyridine; dmap; sodium azide; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1039/c3cc46646a

Reference yield:

: 924895-17-0
(3S,4R,5R,6R)-benzyl 3,4,5-tris(benzyloxy)-6-hydroxyazepane-1-carboxylate

: 1147551-56-1
(3S,4R,5R,6S)-3-azido-4,5,6-tris(benzyloxy)azepane-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: dmap; pyridine / 0 - 20 °C / Inert atmosphere

2: sodium azide / N,N-dimethyl-formamide / 96 h / 90 °C

With pyridine; dmap; sodium azide; In N,N-dimethyl-formamide;
DOI:10.1039/c3cc46646a