(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

Base Information

Chemical Name:(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide
CAS No.:1159610-21-5
Molecular Formula:C₁₉H₁₉ClN₄O₄S
Molecular Weight:434.903
Hs Code.:

Synonyms:(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

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Chemical Property of (S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

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Technology Process of (S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

There total 8 articles about (S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide 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: 55.0%

: 2-(N-methylamino)ethylhydroxylamine hydrochloride

: 1027385-05-2
(S)-5-chloro-N-((3-(4-cyanophenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

: 1159610-21-5
(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

Guidance literature:: (S)-5-chloro-N-((3-(4-cyanophenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide; With hydrogenchloride; In methanol; at 0 - 20 ℃; for 5h;

2-(N-methylamino)ethylhydroxylamine hydrochloride; With acetic acid; for 16h; Reflux;

With sodium carbonate; In water;

Reference yield: 31.0%

: 1027385-05-2
(S)-5-chloro-N-((3-(4-cyanophenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

: 2-(N-methylamino)ethyl-hydroxylamine hydrochloride

: 1159610-21-5
(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

Guidance literature:: (S)-5-chloro-N-((3-(4-cyanophenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide; With hydrogenchloride; In methanol; at 0 - 20 ℃; for 3h;

2-(N-methylamino)ethyl-hydroxylamine hydrochloride; In methanol; acetic acid; Reflux;

Reference yield:

: 873-74-5
4-Aminobenzonitrile

: 1159610-21-5
(S)-5-chloro-N-((3-(4-(5,6-dihydro-4H-1,2,4-oxadiazin-3-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)thiophene-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: 13 h / 105 °C

2.1: dmap / N,N-dimethyl-formamide / 36 h / 80 - 90 °C

3.1: hydrazine hydrate / dichloromethane; methanol / 5 h / Reflux

4.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 4-hydroxybenzotriazole / N,N-dimethyl-formamide / 15 h / 0 - 20 °C

5.1: hydrogenchloride / methanol / 5 h / 0 - 20 °C

5.2: 16 h / Reflux

With hydrogenchloride; 4-hydroxybenzotriazole; hydrazine hydrate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; dmap; In methanol; dichloromethane; N,N-dimethyl-formamide;