2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid

Base Information

• Chemical Name: 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid
• CAS No.: 528891-38-5
• Molecular Formula: C₂₃H₃₅N₃O₆
• Molecular Weight: 449.547

Synonyms:2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid

Chemical Property of 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid

Chemical Property:

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Technology Process of 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid

There total 3 articles about 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid 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: 86.0%

Boc-L-Phe-L-Ala-L-Leu-OMe (70396-33-7) → 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid (528891-38-5)

Guidance literature:

With lithium hydroxide; In methanol; water; at 20 ℃; for 3h;

DOI:10.1016/S0040-4039(02)02573-X

Reference yield:

N-tert-butyloxycarbonyl-L-phenylalanyl-L-alanine (55677-48-0) → 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid (528891-38-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: iBuOOCCl; Et₃N / CH₂Cl₂ / 0.08 h / 0 °C

1.2: 65 percent / Et₃N / CH₂Cl₂ / 8 h

2.1: 86 percent / LiOH / methanol; H₂O / 3 h / 20 °C

With lithium hydroxide; triethylamine; isobutyl chloroformate; In methanol; dichloromethane; water;

DOI:10.1016/S0040-4039(02)02573-X

Reference yield:

methyl (L)-leucinate hydrochloride (7517-19-3) → 2-[2-(2-tert-butoxycarbonylamino-3-phenyl-propionylamino)-propionylamino]-4-methyl-pentanoic acid (528891-38-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: iBuOOCCl; Et₃N / CH₂Cl₂ / 0.08 h / 0 °C

1.2: 65 percent / Et₃N / CH₂Cl₂ / 8 h

2.1: 86 percent / LiOH / methanol; H₂O / 3 h / 20 °C

With lithium hydroxide; triethylamine; isobutyl chloroformate; In methanol; dichloromethane; water;

DOI:10.1016/S0040-4039(02)02573-X

upstream raw materials:

Boc-L-Phe-L-Ala-L-Leu-OMe

N-tert-butyloxycarbonyl-L-phenylalanyl-L-alanine

methyl (L)-leucinate hydrochloride

Downstream raw materials:

(1-{1-[1-(3-bromo-benzylcarbamoyl)-3-methyl-butylcarbamoyl]-ethylcarbamoyl}-2-phenyl-ethyl)-carbamic acid tert-butyl ester

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