tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

Base Information

Chemical Name:tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate
CAS No.:1380494-52-9
Molecular Formula:C₂₅H₃₄FN₃O₈S
Molecular Weight:555.625
Hs Code.:

tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

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Chemical Property of tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

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Technology Process of tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

There total 7 articles about tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate 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:

: 36016-38-3
tert-Butyl N-hydroxycarbamate

: 1380494-52-9
tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium periodate / methanol; water / 8 h / 20 °C / Inert atmosphere

2.1: 20% palladium hydroxide-activated charcoal; hydrogen / methanol / 8 h / 20 °C / 2585.81 Torr

3.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C / Inert atmosphere

4.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

5.1: sodium hydrogencarbonate / tetrahydrofuran; water / 1 h / 0 °C / Inert atmosphere

6.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C / Inert atmosphere

6.2: -78 - 25 °C / Inert atmosphere

7.1: triethylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere

With sodium periodate; n-butyllithium; palladium 10% on activated carbon; 20% palladium hydroxide-activated charcoal; hydrogen; sodium hydrogencarbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmc.2012.04.026

Reference yield:

: tert-butyl 1'-(2-fluoro-4-nitrophenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

: 1380494-52-9
tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

2.1: sodium hydrogencarbonate / tetrahydrofuran; water / 1 h / 0 °C / Inert atmosphere

3.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C / Inert atmosphere

3.2: -78 - 25 °C / Inert atmosphere

4.1: triethylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere

With n-butyllithium; palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; triethylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; water;
DOI:10.1016/j.bmc.2012.04.026

Reference yield:

: 1'-benzyl 3-tert-butyl 2-oxa-3-azaspiro[bicyclo[2.2.1]hept[5]ene-7,4'-piperidine]-1',3-dicarboxylate

: 1380494-52-9
tert-butyl 1'-(2-fluoro-4-((R)-5-((methylsulfonyloxy)methyl)-2-oxooxazolidin-3-yl)phenyl)-2-oxa-3-azaspiro[bicyclo[2.2.1]heptane-7,4'-piperidine]-3-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 20% palladium hydroxide-activated charcoal; hydrogen / methanol / 8 h / 20 °C / 2585.81 Torr

2.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 18 h / 20 °C / Inert atmosphere

3.1: palladium 10% on activated carbon; hydrogen / methanol / 4 h / 20 °C / 760.05 Torr

4.1: sodium hydrogencarbonate / tetrahydrofuran; water / 1 h / 0 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran; hexane / 0.25 h / -78 °C / Inert atmosphere

5.2: -78 - 25 °C / Inert atmosphere

6.1: triethylamine / dichloromethane / 18 h / 20 °C / Inert atmosphere

With n-butyllithium; palladium 10% on activated carbon; 20% palladium hydroxide-activated charcoal; hydrogen; sodium hydrogencarbonate; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; hexane; dichloromethane; water; acetonitrile;
DOI:10.1016/j.bmc.2012.04.026