{2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

Base Information

Chemical Name:{2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester
CAS No.:1452466-20-4
Molecular Formula:C₁₄H₂₄N₄O₆
Molecular Weight:344.368
Hs Code.:

Synonyms:{2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

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Chemical Property of {2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

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Technology Process of {2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

There total 1 articles about {2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester 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:

: 63088-78-8,448964-01-0,478409-64-2
(2S,5R)-5-hydroxypiperidine-2-carboxylic acid

: 1452466-20-4
{2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 10 steps

1.1: hydrogenchloride / 3 h / Reflux

2.1: triethylamine / tetrahydrofuran / 2.17 h / 10 - 20 °C / Cooling with ice

3.1: 2,6-dimethylpyridine; trifluoromethylsulfonic anhydride / acetonitrile / 0.67 h / -36 - -30 °C

3.2: 48 h / -32 - 4 °C

4.1: hydrogenchloride / methanol / 72 h / Reflux

5.1: potassium carbonate / ethyl acetate; water

6.1: sodium hydroxide; water / 1,4-dioxane / 1 h / Cooling with ice

6.2: 20 °C

7.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane / 20 °C / Cooling with ice

8.1: hydrogenchloride / 1,4-dioxane / 2 h / Cooling with ice

9.1: triethylamine; chloro-trimethyl-silane / acetonitrile / 1 h / Cooling with ice

9.2: 0.33 h

9.3: 20 °C

10.1: palladium 10% on activated carbon; hydrogen / water; tetrahydrofuran / 3 h

With 2,6-dimethylpyridine; hydrogenchloride; chloro-trimethyl-silane; trifluoromethylsulfonic anhydride; palladium 10% on activated carbon; water; hydrogen; potassium carbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; water; ethyl acetate; acetonitrile;

Reference yield:

: 1452466-20-4
{2-[({[(2S,5R)-6-hydroxy-7-oxo-1,6-diazabicyclo[3.2.1]oct-2-yl]carbonyl}amino)oxy]ethyl}carbamic acid tert-butyl ester

: 1452458-86-4
RG₆₀₈₀

Guidance literature:: Multi-step reaction with 2 steps

1: sulfur trioxide pyridine complex / pyridine / 23 h / 20 °C

2: trifluoroacetic acid / dichloromethane / 1 h / 0 °C

With sulfur trioxide pyridine complex; trifluoroacetic acid; In pyridine; dichloromethane;