3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

Base Information

Chemical Name:3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate
CAS No.:1429913-71-2
Molecular Formula:C₁₇H₂₆N₂O₇S
Molecular Weight:402.469
Hs Code.:

Synonyms:3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

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Chemical Property of 3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

Chemical Property:

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Technology Process of 3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

There total 3 articles about 3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate 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:

: 1429913-70-1,1263045-28-8
benzyl tert-butyl (3-hydroxypropane-1,2-diyl)biscarbamate

: 124-63-0
methanesulfonyl chloride

: 1429913-71-2
3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

Guidance literature:: In dichloromethane; at 0 - 20 ℃; for 12h;

Reference yield:

: 76387-70-7
(S)-3-amino-2-tert-butoxycarbonylaminopropionic acid

: 1429913-71-2
3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate; potassium hydroxide / tetrahydrofuran; water / 16 h / 0 - 20 °C

2: potassium carbonate / dimethyl sulfoxide / 12 h / 20 °C

3: lithium borohydride / tetrahydrofuran / 1 h / 0 - 20 °C

4: dichloromethane / 12 h / 0 - 20 °C

With lithium borohydride; potassium carbonate; potassium hydroxide; In tetrahydrofuran; dichloromethane; water; dimethyl sulfoxide;

Reference yield:

: 61040-22-0
N^β-benzyloxycarbonyl-N^α-Boc-(R)-β-aminoalanine methyl ester

: 1429913-71-2
3-{[(benzyloxy)carbonyl]amino}-2-[(tert-butoxycarbonyl)amino]propyl methanesulfonate

Guidance literature:: Multi-step reaction with 2 steps

1: lithium borohydride / tetrahydrofuran / 1 h / 0 - 20 °C

2: dichloromethane / 12 h / 0 - 20 °C

With lithium borohydride; In tetrahydrofuran; dichloromethane;