(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Base Information

Chemical Name:(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester
CAS No.:719308-13-1
Molecular Formula:C₂₁H₂₁N₃O₅
Molecular Weight:395.415
Hs Code.:

Synonyms:(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Suppliers and Price of (2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl 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 (2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

There total 3 articles about (2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl 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: 33.0%

: 719307-96-7
4-(N'-benzoyl-hydrazino)-(2S)-2-benzyloxycarbonylamino-4-oxo-butyric acid ethyl ester

: 719308-13-1
(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Guidance literature:: 4-(N'-benzoyl-hydrazino)-(2S)-2-benzyloxycarbonylamino-4-oxo-butyric acid ethyl ester; With 2-chloro-1,3-dimethylimidazolinium tetrafluoroborate; triethylamine; In dichloromethane;

In toluene; at 80 ℃;
DOI:10.1016/j.bmcl.2011.03.109

Reference yield:

: C₁₄H₁₆ClNO₅

: 719308-13-1
(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: pyridine / dichloromethane

2.1: 2-chloro-1,3-dimethylimidazolinium tetrafluoroborate; triethylamine / dichloromethane

2.2: 80 °C

With 2-chloro-1,3-dimethylimidazolinium tetrafluoroborate; pyridine; triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2011.03.109

Reference yield:

: 4668-43-3
(S)-3-(benzyloxycarbonylamino)-4-ethoxy-4-oxobutanoic acid

: 719308-13-1
(2S)-2-benzyloxycarbonylamino-3-(5-phenyl-[1,3,4]oxadiazol-2-yl)-propionic acid ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide

2.1: pyridine / dichloromethane

3.1: 2-chloro-1,3-dimethylimidazolinium tetrafluoroborate; triethylamine / dichloromethane

3.2: 80 °C

With 2-chloro-1,3-dimethylimidazolinium tetrafluoroborate; pyridine; oxalyl dichloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2011.03.109