(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

Base Information

Chemical Name:(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester
CAS No.:92514-79-9
Molecular Formula:C₄₃H₅₅N₇O₁₂
Molecular Weight:861.949
Hs Code.:

(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

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Chemical Property of (S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

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Technology Process of (S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

There total 5 articles about (S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester 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:

: 24498-31-5
(S)-methyl 2-amino-6-(benzyloxycarbonylamino)hexanoate

: 92514-79-9
(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) isobutyl chloroformate, triethylamine / DMF, 1.) -13 deg C, 15 min, 2.) -13 deg C, 30 min, 0 deg C, 1 h, then room temperature, 3 days

2: 85 percent / HCl / methanol; ethanol / 24 h / Ambient temperature

3: 1.) triethylamine / 1.) chloroform, 20 min, 2.) DMF-chloroform, -12 deg C, 1 h, 0 deg C, 3 h, then room temperature, 3 h

With hydrogenchloride; triethylamine; isobutyl chloroformate; In methanol; ethanol;

Reference yield:

: 23380-20-3
N^α-formylglycyl-glycyl-glycine

: 92514-79-9
(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) isobutyl chloroformate, triethylamine / DMF, 1.) -13 deg C, 15 min, 2.) -13 deg C, 30 min, 0 deg C, 1 h, then room temperature, 3 days

2: 85 percent / HCl / methanol; ethanol / 24 h / Ambient temperature

3: 1.) triethylamine / 1.) chloroform, 20 min, 2.) DMF-chloroform, -12 deg C, 1 h, 0 deg C, 3 h, then room temperature, 3 h

With hydrogenchloride; triethylamine; isobutyl chloroformate; In methanol; ethanol;

Reference yield:

: 74283-31-1
di-Z-L-lysine hydrazide

: 92514-79-9
(S)-6-Benzyloxycarbonylamino-2-(2-{2-[2-((S)-2,6-bis-benzyloxycarbonylamino-hexanoylamino)-acetylamino]-acetylamino}-acetylamino)-hexanoic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: HCl, NaNO₂ / H₂O; acetic acid / 0.17 h / -10 - -5 °C

2: 1.) triethylamine / 1.) chloroform, 20 min, 2.) DMF-chloroform, -12 deg C, 1 h, 0 deg C, 3 h, then room temperature, 3 h

With hydrogenchloride; triethylamine; sodium nitrite; In water; acetic acid;