(S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

Base Information

Chemical Name:(S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate
CAS No.:1489240-39-2
Molecular Formula:C₁₈H₂₃F₂N₅O₄S
Molecular Weight:443.475
Hs Code.:

Synonyms:(S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

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Technology Process of (S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

There total 2 articles about (S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate 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:

: C₂₃H₃₁F₂N₅O₆S

: 1489240-39-2
(S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

Guidance literature:: With hydrogenchloride; water; In 1,4-dioxane; at 20 ℃; for 2h;
DOI:10.1016/j.ejmech.2013.08.002

Reference yield:

: 952151-87-0
O-methyl (S)-N-(3-(4-(1-(tert-butoxycarbonyl)[1,2,5]triazepan-5-yl)-3,5-difluorophenyl)-2-oxooxazolidin-5-yl)methylthiocarbamate

: 1489240-39-2
(S)-N-((3-(3,5-difluoro-4-(1-acetyl[1,2,5]triazepan-5-yl)phenyl)-2-oxo-5-oxazolidinyl)methyl)-O-methylthiocarbamate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0.5 h / 20 °C

2: hydrogenchloride; water / 1,4-dioxane / 2 h / 20 °C

With hydrogenchloride; water; triethylamine; In 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2013.08.002