N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

Base Information

Chemical Name:N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester
CAS No.:109924-32-5
Molecular Formula:C₁₈H₂₇N₃O₃S
Molecular Weight:365.497
Hs Code.:

Synonyms:N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

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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 N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

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Technology Process of N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

There total 3 articles about N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester 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:

: 3674-06-4
Boc-Phe-ONSu

: 109924-32-5
N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

Guidance literature:: Multi-step reaction with 3 steps

1: 84 percent / NaOH / dioxane; H₂O / Ambient temperature

2: 83 percent / LiOEt, H₂S / ethanol / Ambient temperature

3: CH₂Cl₂ / Ambient temperature

With sodium hydroxide; hydrogen sulfide; lithium ethoxide; In 1,4-dioxane; ethanol; dichloromethane; water;
DOI:10.1002/hlca.19860690530

Reference yield:

: 109924-24-5
tert-butyl-(1-((cyanomethyl)amino)-1-oxo-3-phenylpropan-2-yl)carbamate

: 109924-32-5
N-(tert-Butoxycarbonyl)-L-phenylalanyl-glycin-imidthiosaeure-S-ethylester

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / LiOEt, H₂S / ethanol / Ambient temperature

2: CH₂Cl₂ / Ambient temperature

With hydrogen sulfide; lithium ethoxide; In ethanol; dichloromethane;
DOI:10.1002/hlca.19860690530