N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

Base Information

Chemical Name:N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine
CAS No.:128404-11-5
Molecular Formula:C₂₂H₃₃N₃O₈
Molecular Weight:467.519
Hs Code.:

N<sup>α</sup>-benzyloxycarbonyl-N<sup>ε</sup>-tert-butyloxycarbonyl-lysyl-serine

Synonyms:N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

Suppliers and Price of N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

There total 1 articles about N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine 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: 88.0%

: 56-45-1,83245-15-2
L-serin

: 2212-69-3
N₂-benzyloxycarbonyl-N₆-t-butoxycarbonyl-L-lysine 4-nitrophenyl ester

: 128404-11-5
N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

Guidance literature:: With N-benzyl-trimethylammonium hydroxide; In N,N-dimethyl-formamide; for 24h; Ambient temperature;

Reference yield:

: 128404-11-5
N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

: 128404-16-0
{2-[((S)-1-{(S)-2-[(S)-2-(2-Benzyloxycarbonylamino-acetylamino)-6-tert-butoxycarbonylamino-hexanoylamino]-3-hydroxy-propionyl}-pyrrolidine-2-carbonyl)-amino]-acetylamino}-acetic acid benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, 2.) 1N NaOH / 1.) Pd-C / 1.) MeOH, H₂O, 2.) dioxane, RT, 1 day

2: 1.) CF₃COOH, 2.) diphenylphosphoryl azide, N-ethylmorpholine / 1.) CH₂Cl₂, 0 deg C, 2.) DMF, 0 deg C, then RT

With N-ethylmorpholine;; sodium hydroxide; diphenylphosphoranyl azide; hydrogen; trifluoroacetic acid; palladium on activated charcoal;

Reference yield:

: 128404-11-5
N^α-benzyloxycarbonyl-N^ε-tert-butyloxycarbonyl-lysyl-serine

: 128404-15-9
N-benzyloxycarbonylglycyl-N^ε-tert-butyloxycarbonyl-lysyl-seryl-glutamyl-glycylglycine benzylester

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) H₂, 2.) 1N NaOH / 1.) Pd-C / 1.) MeOH, H₂O, 2.) dioxane, RT, 1 day

2: 1.) CF₃COOH, 2.) diphenylphosphoryl azide, N-ethylmorpholine / 1.) CH₂Cl₂, 0 deg C, 40 min, 2.) DMF, 0 deg C, 1h, then RT, 20h

With N-ethylmorpholine;; sodium hydroxide; diphenylphosphoranyl azide; hydrogen; trifluoroacetic acid; palladium on activated charcoal;