C₃₉H₃₈ClFN₄O₉S

Base Information

Chemical Name:C₃₉H₃₈ClFN₄O₉S
CAS No.:1100292-32-7
Molecular Formula:C₃₉H₃₈ClFN₄O₉S
Molecular Weight:793.27
Hs Code.:

C<sub>39</sub>H<sub>38</sub>ClFN<sub>4</sub>O<sub>9</sub>S

Synonyms:C₃₉H₃₈ClFN₄O₉S

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Chemical Property of C₃₉H₃₈ClFN₄O₉S

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Technology Process of C₃₉H₃₈ClFN₄O₉S

There total 11 articles about C₃₉H₃₈ClFN₄O₉S 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: 8.0%

: 1093628-41-1
5-chloro-N-({(5S)-3-[2-fluoro-4-(3-oxomorpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)thiophene-2-carboxamide

: 947181-39-7
Benzyl (4-chloro-4-oxobutyl)(4-methoxybenzyl)carbamate

: 1100292-32-7
C₃₉H₃₈ClFN₄O₉S

Guidance literature:: 5-chloro-N-({(5S)-3-[2-fluoro-4-(3-oxomorpholin-4-yl)phenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)thiophene-2-carboxamide; With sodium hydride; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h; Inert atmosphere;

Benzyl (4-chloro-4-oxobutyl)(4-methoxybenzyl)carbamate; In N,N-dimethyl-formamide; Inert atmosphere;

With hydrogenchloride; In dichloromethane; at 20 ℃; for 20h;

Reference yield:

: 29632-74-4
2-fluro-4-iodoaniline

: 1100292-32-7
C₃₉H₃₈ClFN₄O₉S

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetra-(n-butyl)ammonium iodide; sodium carbonate / dichloromethane; water / 144 h / Reflux

2.1: potassium phosphate; copper(l) iodide; N,N`-dimethylethylenediamine / 1,4-dioxane / 15 h / Inert atmosphere; Reflux

3.1: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 20 °C / 750.08 Torr

4.1: magnesium(II) perchlorate / acetonitrile / 15 h / 20 °C

5.1: dmap / propyl cyanide / 72 h / 70 °C

6.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

6.2: 0.25 h / 20 °C / Inert atmosphere

With dmap; potassium phosphate; copper(l) iodide; magnesium(II) perchlorate; hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; sodium carbonate; N,N`-dimethylethylenediamine; palladium 10% on activated carbon; In 1,4-dioxane; propyl cyanide; ethanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1093628-67-1
N,N-Dibenzyl-2-fluoro-4-iodoaniline

: 1100292-32-7
C₃₉H₃₈ClFN₄O₉S

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium phosphate; copper(l) iodide; N,N`-dimethylethylenediamine / 1,4-dioxane / 15 h / Inert atmosphere; Reflux

2.1: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 20 °C / 750.08 Torr

3.1: magnesium(II) perchlorate / acetonitrile / 15 h / 20 °C

4.1: dmap / propyl cyanide / 72 h / 70 °C

5.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 20 °C / Inert atmosphere

5.2: 0.25 h / 20 °C / Inert atmosphere

With dmap; potassium phosphate; copper(l) iodide; magnesium(II) perchlorate; hydrogen; sodium hydride; N,N`-dimethylethylenediamine; palladium 10% on activated carbon; In 1,4-dioxane; propyl cyanide; ethanol; N,N-dimethyl-formamide; acetonitrile;