benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

Base Information

Chemical Name:benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester
CAS No.:76491-44-6
Molecular Formula:C₂₈H₄₂N₆O₉
Molecular Weight:606.676
Hs Code.:

benzyloxycarbonylalanyl-D-isoglutaminyl-N<sup>ε</sup>-acetyllysyl-D-alanine methyl ester

Synonyms:benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

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Chemical Property of benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

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Technology Process of benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

There total 4 articles about benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine 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:

: 1168-87-2
benzyloxycarbonylalanine p-nitrophenyl ester

: 76491-44-6
benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / NaOH / dimethylformamide; H₂O / 12 h

With sodium hydroxide; In water; N,N-dimethyl-formamide;

Reference yield:

: 63648-75-9
D-isoglutamine hydrobromide

: 76491-44-6
benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / NaOH / dimethylformamide; H₂O / 12 h

With sodium hydroxide; In water; N,N-dimethyl-formamide;

Reference yield:

: 68223-08-5
(R)-6-acetylamino-2-benzyloxycarbonylaminohexanoic acid

: 76491-44-6
benzyloxycarbonylalanyl-D-isoglutaminyl-N^ε-acetyllysyl-D-alanine methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 1. N-ethylpiperidine, pivaloyl chloride / 1. 0 deg C, 5 min, CHCl₃; 2. 0 deg C, CHCl₃

With 1-ethyl-piperidine; pivaloyl chloride;