(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Base Information

Chemical Name:(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide
CAS No.:1244610-62-5
Molecular Formula:C₁₉H₂₂N₄O₅
Molecular Weight:386.407
Hs Code.:

Synonyms:(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Suppliers and Price of (S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Chemical Property:

Purity/Quality:

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Technology Process of (S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

There total 4 articles about (S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide 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:

: 26416-38-6,118758-09-1,16859-11-3
2-[3-(1-methoxycarbonyl-2-phenylethyl)ureido]-3-phenylpropionic acid methyl ester

: 1244610-62-5
(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Guidance literature:: With hydroxylamine potassium salt; In methanol; at 20 ℃; for 5h;
DOI:10.1016/j.bmc.2012.04.035

Reference yield:

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: 1244610-62-5
(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetyl chloride / Reflux

2: triethylamine / dichloromethane / 0.5 h / 20 °C / Cooling with ice

3: hydroxylamine potassium salt / methanol / 5 h / 20 °C

With hydroxylamine potassium salt; triethylamine; acetyl chloride; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2012.04.035

Reference yield:

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 1244610-62-5
(S,S)-N-hydroxy-2-[3-(1-hydroxycarbamoyl-2-phenylethyl)-ureido]-3-phenyl-propionamide

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / dichloromethane / 0.25 h / Cooling with ice

2: triethylamine / dichloromethane / 0.5 h / 20 °C / Cooling with ice

3: hydroxylamine potassium salt / methanol / 5 h / 20 °C

With hydroxylamine potassium salt; sodium hydrogencarbonate; triethylamine; In methanol; dichloromethane;
DOI:10.1016/j.bmc.2012.04.035