[(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

Base Information

Chemical Name:[(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid
CAS No.:236123-26-5
Molecular Formula:C₁₇H₃₀N₂O₄Si
Molecular Weight:354.522
Hs Code.:

Synonyms:[(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

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Chemical Property of [(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

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Technology Process of [(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

There total 1 articles about [(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid 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: 96.0%

: 236123-25-4
benzyl [(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylate

: 236123-26-5
[(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 25 ℃; for 0.5h; under 760.051 Torr;

Reference yield: 80.0%

: 236123-26-5
[(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid

: 7531-52-4
L-prolinamide

: 236123-27-6
N₁-[1-[N-[(S)-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarbonyl]-L-prolinamide

Guidance literature:: [(S)-1-[N-tert-butyldimethylsilyl-4-oxo-azetidine-2-carbonyl]amino]cyclohexanecarboxylic acid; With 2,3,4,5,6-pentafluorophenol; dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; at 0 ℃; for 1.5h;

L-prolinamide; In N,N-dimethyl-formamide; at 20 ℃; for 2h;