(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

Base Information

Chemical Name:(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester
CAS No.:141437-98-1
Molecular Formula:C₃₆H₄₆N₂O₅S₃
Molecular Weight:682.97
Hs Code.:

(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

Synonyms:(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

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Chemical Property of (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

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Technology Process of (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

There total 13 articles about (S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester 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: 65.0%

: 141437-96-9
[(S)-3-Methylsulfanyl-1-(pyridin-2-yldisulfanylmethyl)-propyl]-carbamic acid tert-butyl ester

: 135949-97-2
(S)-2-(2-Mercaptomethyl-3-phenyl-propionylamino)-3-phenyl-propionic acid benzyl ester

: 141437-98-1
(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

Guidance literature:: In ethanol; Ambient temperature;
DOI:10.1021/jm00091a016

Reference yield:

: 139429-04-2
Thioacetic acid S-((S)-2-tert-butoxycarbonylamino-4-methylsulfanyl-butyl) ester

: 141437-98-1
(S)-2-[(S)-2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / 1 M NaOH / ethanol / 3 h / 0 - 20 °C

2: 75 percent / CH₃COOH / ethanol / Ambient temperature

3: ethanol / Ambient temperature

With sodium hydroxide; acetic acid; In ethanol;
DOI:10.1021/jm00091a016

Reference yield:

: 141437-94-7
((S)-1-Mercaptomethyl-3-methylsulfanyl-propyl)-carbamic acid tert-butyl ester

: 141437-98-1
(S)-2-[2-((S)-2-tert-Butoxycarbonylamino-4-methylsulfanyl-butyldisulfanylmethyl)-3-phenyl-propionylamino]-3-phenyl-propionic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / CH₃COOH / ethanol / Ambient temperature

2: 65 percent / ethanol / Ambient temperature

With acetic acid; In ethanol;
DOI:10.1021/jm00091a016