(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

Base Information

Chemical Name:(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate
CAS No.:1444001-53-9
Molecular Formula:C₂₇H₃₁N₅O₆
Molecular Weight:521.573
Hs Code.:

Synonyms:(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

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Chemical Property of (R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

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Technology Process of (R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

There total 11 articles about (R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate 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: 19.0%

: 1444001-38-0
(R)-ethyl 1-(4-(5-(aminomethyl)-2-oxooxazolidin-3-yl)phenyl)piperidine-4-carboxylate

: 1444001-64-2
4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzaldehyde

: 1444001-53-9
(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

Guidance literature:: With sodium tris(acetoxy)borohydride; In N,N-dimethyl-formamide; at 20 ℃; for 15h;
DOI:10.1016/j.ejmech.2013.03.056

Reference yield:

: 1444001-33-5
(R)-ethyl 1-(4-(5-((1,3-dioxoisoindolin-2-yl)methyl)-2-oxooxazolidin-3-yl)phenyl)piperidine-4-carboxylate

: 1444001-53-9
(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: hydrazine hydrate / ethanol / 2.5 h / 0 - 80 °C

2: sodium tris(acetoxy)borohydride / N,N-dimethyl-formamide / 15 h / 20 °C

With sodium tris(acetoxy)borohydride; hydrazine hydrate; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2013.03.056

Reference yield:

: 66739-89-7
4-(1,3-dioxolan-2-yl)benzonitrile

: 1444001-53-9
(R)-ethyl 1-(4-(2-oxo-5-(((4-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)benzyl)amino)methyl)oxazolidin-3-yl)phenyl)piperidine-4-carboxylate

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine; hydroxylamine hydrochloride / ethanol / 15 h / 60 °C

2: triethylamine / dichloromethane / 4 h / -10 - 20 °C

3: N,N-dimethyl-formamide / 0.25 h / 140 °C / Microwave irradiation

4: pyridinium p-toluenesulfonate / acetone; water / 6 h / Reflux

5: sodium tris(acetoxy)borohydride / N,N-dimethyl-formamide / 15 h / 20 °C

With hydroxylamine hydrochloride; pyridinium p-toluenesulfonate; sodium tris(acetoxy)borohydride; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2013.03.056