trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Base Information

Chemical Name:trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester
CAS No.:1426572-86-2
Molecular Formula:C₂₀H₃₀N₄O₅
Molecular Weight:406.482
Hs Code.:

Synonyms:trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Suppliers and Price of trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

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 trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

There total 4 articles about trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic 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: 88.0%

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

: 108-24-7
acetic anhydride

: 1426572-86-2
trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With triethylamine; In dichloromethane; at 0 - 35 ℃; for 4h;

Reference yield:

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

: 1426572-86-2
trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

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

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

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

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

Reference yield:

: 1426573-07-0
(2S,5R)-1-[(1,1-dimethylethyl)carbonyl]-5-[(benzyloxy)amino]piperidine-2-carboxylic acid

: 1426572-86-2
trans-5-(benzyloxyamino)-2-(N-acetyloxycarbimidoyl)piperidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; pivaloyl chloride / dichloromethane / 1.5 h

1.2: 0.67 h / -40 °C

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

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

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

With hydroxylamine hydrochloride; pivaloyl chloride; sodium hydrogencarbonate; triethylamine; trifluoroacetic anhydride; In methanol; dichloromethane;