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cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine

Base Information
  • Chemical Name:cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine
  • CAS No.:440353-79-7
  • Molecular Formula:C35H56N8O6
  • Molecular Weight:684.88
  • Hs Code.:
cyclo-N<sup>ε</sup>-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine

Synonyms:cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine

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Chemical Property of cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine
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Technology Process of cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine

There total 8 articles about cyclo-Nε-(benzyloxycarbonyl)-L-lysyl-L-valyl-(2-azido-3-undecyl-β-alanyl)glycine 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:
Guidance literature:
With diphenylphosphoranyl azide; sodium hydrogencarbonate; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 53h;
DOI:10.1021/jo016276m
Guidance literature:
Multi-step reaction with 4 steps
1: 180 mg / EDAC*HCl; 1-hydroxy-7-azabenzotriazole / tetrahydrofuran / 54 h / 20 °C
2: 82 percent / LiOH / tetrahydrofuran; methanol; H2O / 3.5 h / 0 - 20 °C
3: 94 percent / 0.5 h / 0 °C
4: 85 percent / NaHCO3; diphenylphosphoryl azide / dimethylformamide / 53 h / 0 - 20 °C
With lithium hydroxide; 1-hydroxy-7-aza-benzotriazole; diphenylphosphoranyl azide; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/jo016276m
Guidance literature:
Multi-step reaction with 7 steps
1: 82 percent / 4-dimethylaminopyridine / acetonitrile / 0.33 h
2: 84 percent / diisopropylethylamine; sodium azide / dimethylformamide / 20 °C
3: hydrogen chloride / diethyl ether / 0.5 h
4: 180 mg / EDAC*HCl; 1-hydroxy-7-azabenzotriazole / tetrahydrofuran / 54 h / 20 °C
5: 82 percent / LiOH / tetrahydrofuran; methanol; H2O / 3.5 h / 0 - 20 °C
6: 94 percent / 0.5 h / 0 °C
7: 85 percent / NaHCO3; diphenylphosphoryl azide / dimethylformamide / 53 h / 0 - 20 °C
With hydrogenchloride; dmap; lithium hydroxide; sodium azide; 1-hydroxy-7-aza-benzotriazole; diphenylphosphoranyl azide; sodium hydrogencarbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; methanol; diethyl ether; water; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/jo016276m
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