5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

Base Information

Chemical Name:5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one
CAS No.:1489240-55-2
Molecular Formula:C₂₃H₂₄FN₇O₅
Molecular Weight:497.486
Hs Code.:

Synonyms:5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

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Chemical Property of 5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

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Technology Process of 5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

There total 4 articles about 5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)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:

: C₂₅H₂₆FN₇O₆

: 1489240-55-2
5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

Guidance literature:: With methanol; potassium carbonate; at 20 ℃; for 0.5h;
DOI:10.1016/j.ejmech.2013.08.002

Reference yield:

: 1489240-56-3
5-(5-bromopyridin-2-yl)[1,2,5]oxadiazepane-2-carboxylic acid tert-butyl ester

: 1489240-55-2
5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 4 steps

1: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / 1,4-dioxane; water / 1.5 h / Reflux

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

3: pyridine / dichloromethane / 2 h

4: potassium carbonate; methanol / 0.5 h / 20 °C

With pyridine; hydrogenchloride; methanol; tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; sodium carbonate; potassium carbonate; In 1,4-dioxane; dichloromethane; water; 1: |Suzuki-Miyaura Coupling;
DOI:10.1016/j.ejmech.2013.08.002

Reference yield:

: 1489240-60-9
5(R)-3-(4-(2-(2-(tert-Butoxycarbonyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

: 1489240-55-2
5(R)-3-(4-(2-(2-(hydroxyacetyl)[1,2,5]oxadiazepan-5-yl)pyridin-5-yl)-3-fluorophenyl)-5-(1,2,3-triazol-1-ylmethyl)oxazolidin-2-one

Guidance literature:: Multi-step reaction with 3 steps

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

2: pyridine / dichloromethane / 2 h

3: potassium carbonate; methanol / 0.5 h / 20 °C

With pyridine; hydrogenchloride; methanol; water; potassium carbonate; In 1,4-dioxane; dichloromethane;
DOI:10.1016/j.ejmech.2013.08.002