N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

Base Information

Chemical Name:N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine
CAS No.:87796-96-1
Molecular Formula:C₃₄H₃₉N₃O₉
Molecular Weight:633.698
Hs Code.:

N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ-<N(ε)-benzyloxycarbonyl>-L-lysine

Synonyms:N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

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Chemical Property of N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

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Technology Process of N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

There total 3 articles about N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine 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: 85.0%

: 87796-95-0
N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine t-butyl ester

: 87796-96-1
N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

Guidance literature:: With water; In trifluoroacetic acid; for 0.5h; Ambient temperature;

Reference yield:

: 5978-22-3,1426213-63-9
N(ε)-benzoyloxycarbonyl-L-lysine tert-butyl ester hydrochloride

: 87796-96-1
N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / 21 h / Ambient temperature

2: 85 percent / H₂O / trifluoroacetic acid / 0.5 h / Ambient temperature

With water; dicyclohexyl-carbodiimide; In dichloromethane; trifluoroacetic acid;

Reference yield:

: N-benzyloxycarbonyl-D-glutamic acid α-benzyl ester dicyclohexylammonium salt

: 87796-96-1
N-benzyloxycarbonyl-D-glutamyl α-benzyl ester γ--L-lysine

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / N,N'-dicyclohexylcarbodiimide / CH₂Cl₂ / 21 h / Ambient temperature

2: 85 percent / H₂O / trifluoroacetic acid / 0.5 h / Ambient temperature

With water; dicyclohexyl-carbodiimide; In dichloromethane; trifluoroacetic acid;