(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

Base Information

Chemical Name:(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate
CAS No.:1448996-60-8
Molecular Formula:C₂HF₃O₂*C₁₈H₂₂FN₇O₃
Molecular Weight:517.44
Hs Code.:

Synonyms:(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

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Chemical Property of (R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

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Technology Process of (R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

There total 4 articles about (R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate 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: 100.0%

: 1448996-58-4
C₂₃H₃₀FN₇O₅

: 76-05-1
trifluoroacetic acid

: 1448996-60-8
(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

Guidance literature:: In dichloromethane; at 0 - 20 ℃;
DOI:10.1016/j.ejmech.2013.05.041

Reference yield:

: 154590-64-4
(S)-N-[3-[3-fluoro-4-[N-t-butoxycarbonylpiperazin-1-yl]phenyl]-2-oxooxazolidin-5-ylmethyl]azide

: 1448996-60-8
(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1,2-dimethoxyethane / 90 °C

2.1: dichloromethane / 0 - 20 °C

3.1: dicyclohexyl-carbodiimide; benzotriazol-1-ol / dichloromethane / 2 h / 20 °C / Inert atmosphere

3.2: 20 °C / Inert atmosphere

4.1: dichloromethane / 0 - 20 °C

With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In 1,2-dimethoxyethane; dichloromethane;
DOI:10.1016/j.ejmech.2013.05.041

Reference yield:

: 371195-29-8
tert-butyl 4-{2-fluoro-4-[(5R)-2-oxo-5-(1H-1,2,3-triazol-1-ylmethyl)-1,3-oxazolidin-3-yl]phenyl}piperazine-1-carboxylate

: 1448996-60-8
(R)-2-(4-(4-(5-((1H-1,2,3-triazol-1-yl)methyl)-2-oxooxazolidin-3-yl)-2-fluorophenyl) piperazin-1-yl)-2-oxoethanaminium 2,2,2-trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: dichloromethane / 0 - 20 °C

2.1: dicyclohexyl-carbodiimide; benzotriazol-1-ol / dichloromethane / 2 h / 20 °C / Inert atmosphere

2.2: 20 °C / Inert atmosphere

3.1: dichloromethane / 0 - 20 °C

With benzotriazol-1-ol; dicyclohexyl-carbodiimide; In dichloromethane;
DOI:10.1016/j.ejmech.2013.05.041