(S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester

Base Information

• Chemical Name: (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester
• CAS No.: 148528-94-3
• Molecular Formula: C₂₂H₃₄N₂O₇
• Molecular Weight: 438.521

Synonyms:(S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester

Chemical Property of (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester

Chemical Property:

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Technology Process of (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester

There total 2 articles about (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic 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:

Z(OMe)-Leu-OH (23234-83-5) → (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester (148528-94-3)

Guidance literature:

Multi-step reaction with 2 steps

1: NMM / tetrahydrofuran / 0.03 h / -15 °C

2: tetrahydrofuran; dimethylformamide / 3 h / -15 °C

With 4-methyl-morpholine; In tetrahydrofuran; N,N-dimethyl-formamide;

DOI:10.1016/0223-5234(92)90027-X

Reference yield:

C20H29NO7 + (S)-2-Amino-5-methoxy-pentanoic acid methyl ester; hydrochloride → (S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester (148528-94-3)

Guidance literature:

In tetrahydrofuran; N,N-dimethyl-formamide; at -15 ℃; for 3h; Yield given;

DOI:10.1016/0223-5234(92)90027-X

Reference yield: 90.0%

(S)-5-Methoxy-2-[(S)-2-(4-methoxy-benzyloxycarbonylamino)-4-methyl-pentanoylamino]-pentanoic acid methyl ester (148528-94-3) → [(S)-1-((S)-1-Carbamoyl-4-methoxy-butylcarbamoyl)-3-methyl-butyl]-carbamic acid 4-methoxy-benzyl ester (148528-96-5)

Guidance literature:

With ammonia; In methanol;

DOI:10.1016/0223-5234(92)90027-X

upstream raw materials:

Z(OMe)-Leu-OH

Downstream raw materials:

[(S)-1-((S)-1-Carbamoyl-4-methoxy-butylcarbamoyl)-3-methyl-butyl]-carbamic acid 4-methoxy-benzyl ester

Boc-Orn(Boc)-Phe-Phe-Gly-Leu-Nva(5-OCH₃)-NH₂

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