6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester

Base Information

• Chemical Name: 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester
• CAS No.: 401809-99-2
• Molecular Formula: C₂₇H₃₃N₃O₇
• Molecular Weight: 511.575

Synonyms:6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester

Chemical Property of 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester

Chemical Property:

Purity/Quality:

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Technology Process of 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester

There total 1 articles about 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl 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: 88.0%

(4-aminobutyl)carbamic acid benzyl ester (62146-62-7) + 1,3-dioxo-5,7-dihydro-1H,3H-2-oxa-6-aza-s-indacene-6-carboxylic acid tert-butyl ester → 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester (401809-99-2)

Guidance literature:

In N,N-dimethyl-formamide; for 16h;

DOI:10.1021/ja0118789

Reference yield: 87.0%

4-chlorophenylethylamine (156-41-2) + 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester (401809-99-2) → 5-(4-benzyloxycarbonylamino-butylcarbamoyl)-6-[2-(4-chloro-phenyl)-ethylcarbamoyl]-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester

Guidance literature:

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 25 ℃; for 16h;

DOI:10.1021/ja0118789

Reference yield:

[2-(2-thyenyl)ethyl]amine (30433-91-1) + 6-(4-benzyloxycarbonylamino-butylcarbamoyl)-1,3-dihydro-isoindole-2,5-dicarboxylic acid 2-tert-butyl ester (401809-99-2) → 5-(4-benzyloxycarbonylamino-butylcarbamoyl)-6-(2-thiophen-2-yl-ethylcarbamoyl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester

Guidance literature:

With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride;

DOI:10.1021/ja0118789

upstream raw materials:

(4-aminobutyl)carbamic acid benzyl ester

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