methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

Base Information

Chemical Name:methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate
CAS No.:1297471-96-5
Molecular Formula:C₂₇H₃₆N₄O₅
Molecular Weight:496.607
Hs Code.:

Synonyms:methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

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Chemical Property of methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

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Technology Process of methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

There total 6 articles about methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate 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: 98.0%

: 1297471-95-4
methyl (S)-4-methyl-2-[2-[(S)-4-methyl-2-(2-nitrobenzamido)pentanamido]benzamido]pentanoate

: 1297471-96-5
methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; at 20 ℃; for 21h;
DOI:10.3987/COM-10-S(E)58

Reference yield:

: 2666-93-5
(S)-Leu-OMe

: 1297471-96-5
methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

Guidance literature:: Multi-step reaction with 4 steps

1: benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide / tetrahydrofuran / 26 h / 0 - 20 °C

2: water; lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

3: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / chloroform / 17 h / 0 - 20 °C

4: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 21 h / 20 °C

With palladium 10% on activated carbon; water; hydrogen; benzotriazol-1-ol; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; lithium hydroxide; In tetrahydrofuran; chloroform;
DOI:10.3987/COM-10-S(E)58

Reference yield:

: 474089-60-6
methyl (S)-N-(2-nitrobenzoyl)leucinate

: 1297471-96-5
methyl (S)-2-[2-[(S)-2-(2-aminobenzamido)-4-methylpentanamido]benzamido]-4-methylpentanoate

Guidance literature:: Multi-step reaction with 3 steps

1: water; lithium hydroxide / tetrahydrofuran / 1 h / 20 °C

2: N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline / chloroform / 17 h / 0 - 20 °C

3: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 21 h / 20 °C

With palladium 10% on activated carbon; water; hydrogen; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; lithium hydroxide; In tetrahydrofuran; chloroform;
DOI:10.3987/COM-10-S(E)58