N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

Base Information

Chemical Name:N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester
CAS No.:116835-75-7
Molecular Formula:C₂₆H₃₈N₂O₆S
Molecular Weight:506.664
Hs Code.:

Synonyms:N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

Suppliers and Price of N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

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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-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

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Technology Process of N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

There total 1 articles about N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester 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: 90.0%

: 91921-43-6
N-Benzyloxycarbonyl-γ-(S)-glutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

: 116835-75-7
N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

Guidance literature:: With 2,4-(4-phenoxyphenyl)-1,3-dithia-2λ(5),4λ(5)-diphosphetane 2,4-disulfides; In tetrahydrofuran; at 50 ℃; for 48h;

Reference yield:

: 116835-75-7
N-Benzyloxycarbonyl-γ-(S)-thioglutamyl(α-tert.-butylester)-(S)-prolin-tert.-butylester

: 116835-79-1
(2S)-N-<(4S)-4-Benzyloxycarbonylamino-4-(tert.-butoxycarbonyl)butyl>prolin-tert.-butylester

Guidance literature:: With sodium tetrahydroborate; methyl iodide; Yield given. Multistep reaction; 1.) THF, 8 h, reflux; 2.) ethanol, 20 h, r.t.;