(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

Base Information

Chemical Name:(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one
CAS No.:1188400-85-2
Molecular Formula:C₁₇H₂₁F₂N₆O₅P
Molecular Weight:458.362
Hs Code.:

Synonyms:(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

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Chemical Property of (R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

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Technology Process of (R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

There total 8 articles about (R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one 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:

: 1188400-84-1
(R)-methanesulfonic acid 3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-2-oxo-oxazolidin-5-ylmethyl ester

: 1188400-85-2
(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

Guidance literature:: With sodium azide; In N,N-dimethyl-formamide; at 80 ℃;

Reference yield:

: 864072-82-2
1-(2,6-difluoro-4-nitro-phenyl)-piperazine

: 1188400-85-2
(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: trichlorophosphate / dichloromethane / -78 - 0 °C / Inert atmosphere

2.1: n-butyllithium / tetrahydrofuran; hexane / 0 °C / Inert atmosphere

2.2: 20 °C

3.1: hydrogen / palladium 10% on activated carbon / methanol / Inert atmosphere

4.1: sodium hydrogencarbonate / water; acetone; toluene / 0 - 20 °C

5.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere

5.2: 2.08 h / -78 - 20 °C

6.1: triethylamine / dichloromethane / 0 - 20 °C

7.1: sodium azide / N,N-dimethyl-formamide / 80 °C

With n-butyllithium; sodium azide; hydrogen; sodium hydrogencarbonate; triethylamine; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene;

Reference yield:

: 66684-58-0
3,4,5-trifluoronitrobenzene

: 1188400-85-2
(R)-5-azidomethyl-3-{3,5-difluoro-4-[4-(2-oxo-2λ5-[1,3,2]dioxaphosphinan-2-yl)-piperazin-1-yl]-phenyl}-oxazolidin-2-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: acetonitrile / 60 °C

2.1: trichlorophosphate / dichloromethane / -78 - 0 °C / Inert atmosphere

3.1: n-butyllithium / tetrahydrofuran; hexane / 0 °C / Inert atmosphere

3.2: 20 °C

4.1: hydrogen / palladium 10% on activated carbon / methanol / Inert atmosphere

5.1: sodium hydrogencarbonate / water; acetone; toluene / 0 - 20 °C

6.1: n-butyllithium / tetrahydrofuran; hexane / -78 °C / Inert atmosphere

6.2: 2.08 h / -78 - 20 °C

7.1: triethylamine / dichloromethane / 0 - 20 °C

8.1: sodium azide / N,N-dimethyl-formamide / 80 °C

With n-butyllithium; sodium azide; hydrogen; sodium hydrogencarbonate; triethylamine; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; methanol; hexane; dichloromethane; water; N,N-dimethyl-formamide; acetone; toluene; acetonitrile;