6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Base Information

Chemical Name:6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane
CAS No.:1426572-88-4
Molecular Formula:C₁₆H₁₈N₄O₃
Molecular Weight:314.344
Hs Code.:

Synonyms:6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Suppliers and Price of 6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

There total 7 articles about 6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane 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: 48.0%

: 32315-10-9
bis(trichloromethyl) carbonate

: 1426572-89-5
C₁₅H₂₀N₄O₂

: 1426572-88-4
6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Guidance literature:: bis(trichloromethyl) carbonate; C₁₅H₂₀N₄O₂; With triethylamine; In acetonitrile; at 0 - 5 ℃; for 0.5h;

With dmap; In acetonitrile; at 0 - 35 ℃; for 16h;

Reference yield:

: 1426572-83-9
trans-5-(benzyloxyamino)-2-carbamoylpiperidine-1-carboxylic acid tert-butyl ester

: 1426572-88-4
6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine; trifluoroacetic anhydride / dichloromethane / 6 h / 0 - 35 °C

2.1: sodium hydrogencarbonate; hydroxylamine hydrochloride / methanol / 24 h / 0 - 35 °C

3.1: triethylamine / dichloromethane / 4 h / 0 - 35 °C

4.1: pyridine / 6 h / Reflux

5.1: trifluoroacetic acid / dichloromethane / 4 h / -15 - 35 °C

6.1: triethylamine / acetonitrile / 0.5 h / 0 - 5 °C

6.2: 16 h / 0 - 35 °C

With pyridine; hydroxylamine hydrochloride; sodium hydrogencarbonate; triethylamine; trifluoroacetic acid; trifluoroacetic anhydride; In methanol; dichloromethane; acetonitrile;

Reference yield:

: 1426572-85-1
trans-5-(benzyloxyamino)-2-(N-hydroxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

: 1426572-88-4
6-(benzyloxyamino)-2-(5-methyl[1,2,4]oxadiazol-3-yl)-7-oxo-1,6-diazabicyclo[3.2.1]octane

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 4 h / 0 - 35 °C

2.1: pyridine / 6 h / Reflux

3.1: trifluoroacetic acid / dichloromethane / 4 h / -15 - 35 °C

4.1: triethylamine / acetonitrile / 0.5 h / 0 - 5 °C

4.2: 16 h / 0 - 35 °C

With pyridine; triethylamine; trifluoroacetic acid; In dichloromethane; acetonitrile;