(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

Base Information

Chemical Name:(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid
CAS No.:114886-89-4
Molecular Formula:C₂₁H₃₂N₂O₅S
Molecular Weight:424.561
Hs Code.:

Synonyms:(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

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Chemical Property of (S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

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Technology Process of (S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

There total 3 articles about (S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic 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: 94.0%

: 114886-74-7
-L-leucine methyl ester

: 114886-89-4
(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

Guidance literature:: With sodium hydroxide;
DOI:10.1021/jm00119a022

Reference yield:

: 114886-73-6
-L-leucine methyl ester

: 114886-89-4
(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / Lawesson's reagent / benzene / 2 h / Heating

2: 94 percent / aq. NaOH

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

Reference yield:

: 77171-42-7
Boc-epibestatin methyl ester

: 114886-89-4
(S)-2-((2S,3R)-3-tert-Butoxycarbonylamino-2-hydroxy-4-phenyl-thiobutyrylamino)-4-methyl-pentanoic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / N-methylmorpholine, DMAP / ethyl acetate / 1 h / Ambient temperature

2: 71 percent / Lawesson's reagent / benzene / 2 h / Heating

3: 94 percent / aq. NaOH

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