N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide

Base Information

• Chemical Name: N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide
• CAS No.: 215607-28-6
• Molecular Formula: C₃₄H₅₁N₃O₁₀
• Molecular Weight: 661.793

Synonyms:N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide

Chemical Property of N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide

Chemical Property:

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Technology Process of N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide

There total 1 articles about N²-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N¹-methylamide 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: 53.0%

3R-(2,2-Dimethyl-1S-methylcarbamoyl-propylcarbamoyl)-2S-hydroxy-5-methyl-hexanoic acid (191792-13-9) + O-(2,4-dimethoxybenzyl)-N-(2,4,6-trimethoxybenzyl)hydroxylamine (215607-30-0) → N2-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N1-methylamide (215607-28-6)

Guidance literature:

With 2,6-dimethylpyridine; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃;

DOI:10.1021/jm990377j

Reference yield: 84.0%

6-Bromomethyl-coumarin (50465-95-7) + N2-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N1-methylamide (215607-28-6) → N4-(2,4-dimethoxy-benzyloxy)-N1-(2,2-dimethyl-1-methylcarbamoyl-propyl)-2-isobutyl-3-(2-oxo-2H-chromen-6-ylmethoxy)-N4-(2,4,6-trimethoxy-benzyl)-succinamide

Guidance literature:

With 15-crown-5; sodium hydride; In tetrahydrofuran; at 20 ℃; for 3h;

DOI:10.1021/jm990377j

Reference yield:

5-bromomethyl-2-methylbenzothiazole (125872-96-0) + N2-[4-(N-2,4-dimethoxybenzyloxyamino-N-2,4,6-trimethoxybenzylamino)-3S-hydroxy-2R-isobutylsuccinyl]-L-tert-leucine-N1-methylamide (215607-28-6) → N4-(2,4-dimethoxy-benzyloxy)-N1-(2,2-dimethyl-1-methylcarbamoyl-propyl)-2-isobutyl-3-(2-methyl-benzothiazol-5-ylmethoxy)-N4-(2,4,6-trimethoxy-benzyl)-succinamide

Guidance literature:

With 15-crown-5; sodium hydride; In tetrahydrofuran; at 20 ℃;

DOI:10.1021/jm990377j

upstream raw materials:

3R-(2,2-Dimethyl-1S-methylcarbamoyl-propylcarbamoyl)-2S-hydroxy-5-methyl-hexanoic acid

O-(2,4-dimethoxybenzyl)-N-(2,4,6-trimethoxybenzyl)hydroxylamine

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