(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

Base Information

Chemical Name:(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate
CAS No.:1337527-03-3
Molecular Formula:C₂₀H₃₁NO₁₀S₃
Molecular Weight:541.665
Hs Code.:

Synonyms:(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

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Chemical Property of (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

Chemical Property:

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Technology Process of (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

There total 4 articles about (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate 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:

: 1337527-02-2
(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((S)-2,3-dihydroxypropylthio)propanoate

: 124-63-0
methanesulfonyl chloride

: 1337527-03-3
(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

Guidance literature:: With pyridine; dmap; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 1337527-03-3
(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 25 °C

2.1: triethylamine; 1,4-dithio-erythritol / dichloromethane / 1.5 h / 20 °C

3.1: sodium hydroxide / tert-butyl alcohol / 20 °C

3.2: 15 h / 20 °C

4.1: dmap; pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

With pyridine; dmap; 1,4-dithio-erythritol; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In dichloromethane; tert-butyl alcohol;

Reference yield:

: 62574-13-4
L-cystine tert-butyl ester

: 1337527-03-3
(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-( (S)-2,3-bis( methylsulfonyloxy)propylthio)-propanoate

Guidance literature:: Multi-step reaction with 4 steps

1.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 25 °C

2.1: triethylamine; 1,4-dithio-erythritol / dichloromethane / 1.5 h / 20 °C

3.1: sodium hydroxide / tert-butyl alcohol / 20 °C

3.2: 15 h / 20 °C

4.1: dmap; pyridine / dichloromethane / 0 - 20 °C / Inert atmosphere

With pyridine; dmap; 1,4-dithio-erythritol; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In dichloromethane; tert-butyl alcohol;