tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

Base Information

Chemical Name:tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate
CAS No.:895524-77-3
Molecular Formula:C₂₆H₂₇N₅O₅
Molecular Weight:489.531
Hs Code.:

Synonyms:tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

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Chemical Property of tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

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Technology Process of tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

There total 2 articles about tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate 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:

: 895524-76-2
(S)-5-(3-((2-(tert-butoxycarbonylamino)propionylamino)methyl)phenyl)oxazole-4-carboxylic acid hydrazide

: 65-85-0,8013-63-6
benzoic acid

: 895524-77-3
tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In N,N-dimethyl-formamide; at 120 ℃; for 0.25h; Microwave irradiation;

Reference yield:

: C₂₆H₂₉N₅O₆

: 895524-77-3
tert-butyl (S)-1-(3-(4-(5-phenyl-1,3,4-oxadiazol-2-yl)oxazol-5-yl)benzylamino)-1-oxopropan-2-ylcarbamate

Guidance literature:: With diisopropyl-carbodiimide; In N,N-dimethyl-formamide; at 150 ℃; for 0.333333h; Microwave irradiation;
DOI:10.1016/j.bmcl.2009.04.075