Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Base Information

Chemical Name:Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester
CAS No.:148638-81-7
Molecular Formula:C₁₇H₂₇NO₈S₂
Molecular Weight:437.535
Hs Code.:

Synonyms:Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Suppliers and Price of Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl 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 Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

There total 3 articles about Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl 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: 97.0%

: 124-63-0
methanesulfonyl chloride

: 148638-80-6
N-benzyl-N-(tert-butoxycarbonyl)-N-<2(S),3-dihydroxypropyl>amine

: 148638-81-7
Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Guidance literature:: With pyridine; In dichloromethane; a) 0 deg C, 1 h, b) 20-25 deg C, 16 h;

Reference yield:

: 109208-40-4
N-benzyl-N-amine

: 148638-81-7
Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 78 percent / Et₃N / CH₂Cl₂ / 4 h / Ambient temperature

2: 100 percent / 20percent aq. CH₃COOH / 0.83 h / 70 °C

3: 97 percent / pyridine / CH₂Cl₂ / a) 0 deg C, 1 h, b) 20-25 deg C, 16 h

With pyridine; acetic acid; triethylamine; In dichloromethane;

Reference yield:

: 148638-79-3
N-benzyl-N-(tert-butoxycarbonyl)-N-amine

: 148638-81-7
Methanesulfonic acid (S)-2-(benzyl-tert-butoxycarbonyl-amino)-1-methanesulfonyloxymethyl-ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / 20percent aq. CH₃COOH / 0.83 h / 70 °C

2: 97 percent / pyridine / CH₂Cl₂ / a) 0 deg C, 1 h, b) 20-25 deg C, 16 h

With pyridine; acetic acid; In dichloromethane;