-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

Base Information

Chemical Name:-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride
CAS No.:76499-22-4
Molecular Formula:C₂₂H₂₇N₃O₅S₂*ClH
Molecular Weight:514.066
Hs Code.:

<S-<(2-Nitrophenyl)sulfenyl>-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

Synonyms:-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

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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 -L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

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Technology Process of -L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

There total 2 articles about -L-cysteinyl>-L-phenylalanine tert-Butyl Ester 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: 94.0%

: 76499-11-1
<-S-tert-butyl-L-cysteinyl>-L-phenylalanine tert-Butyl Ester

: 76499-22-4
-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; chloroform; for 2h; Ambient temperature;
DOI:10.1021/jo00322a024

Reference yield:

: 15100-75-1,75898-47-4
L-phenylalanine tert-butyl ester hydrochloride

: 76499-22-4
-L-cysteinyl>-L-phenylalanine tert-Butyl Ester Hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / 2-Ethoxy-N-(ethoxycarbonyl)-1,2-dihydroquinoline (EEDQ) / dioxane / 8 h / Ambient temperature

2: 94 percent / HCl / CHCl₃; diethyl ether / 2 h / Ambient temperature

With hydrogenchloride; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In 1,4-dioxane; diethyl ether; chloroform;
DOI:10.1021/jo00322a024