(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

Base Information

Chemical Name:(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride
CAS No.:114886-80-5
Molecular Formula:C₁₅H₂₄N₂OS*ClH
Molecular Weight:316.895
Hs Code.:

Synonyms:(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

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Chemical Property of (2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

Chemical Property:

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Technology Process of (2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

There total 4 articles about (2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride 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%

: 114886-79-2
[(1R,2S)-1-Benzyl-2-hydroxy-2-(3-methyl-butylthiocarbamoyl)-ethyl]-carbamic acid tert-butyl ester

: 114886-80-5
(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

Guidance literature:: With hydrogenchloride;
DOI:10.1021/jm00119a022

Reference yield:

: 114886-77-0
Acetic acid (1S,2R)-2-tert-butoxycarbonylamino-1-(3-methyl-butylcarbamoyl)-3-phenyl-propyl ester

: 114886-80-5
(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: 46 percent / Lawesson's reagent / benzene / 2 h / Heating

2: 81 percent / aq. NaOH

3: 97 percent / HCl

With Lawessons reagent; hydrogenchloride; sodium hydroxide; In benzene;
DOI:10.1021/jm00119a022

Reference yield:

: [(1R,2R)-1-Benzyl-2-hydroxy-2-(3-methyl-butylcarbamoyl)-ethyl]-carbamic acid tert-butyl ester

: 114886-80-5
(2S,3R)-3-Amino-2-hydroxy-N-(3-methyl-butyl)-4-phenyl-thiobutyramide; hydrochloride

Guidance literature:: Multi-step reaction with 4 steps

1: 73 percent / N-methylmorpholine, DMAP / ethyl acetate

2: 46 percent / Lawesson's reagent / benzene / 2 h / Heating

3: 81 percent / aq. NaOH

4: 97 percent / HCl

With Lawessons reagent; 4-methyl-morpholine; hydrogenchloride; dmap; sodium hydroxide; In ethyl acetate; benzene;
DOI:10.1021/jm00119a022