1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni

Base Information

• Chemical Name: 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni
• CAS No.: 101210-32-6
• Molecular Formula: C₄₈H₅₃N₅O₁₅
• Molecular Weight: 939.973

Synonyms:1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni

Chemical Property of 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni

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Technology Process of 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni

There total 11 articles about 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni 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: 82.0%

3-(5-acetoxymethyl-2-formyl-4-methoxycarbonylmethyl-pyrrol-3-yl)-propionic acid methyl ester (58950-46-2) + 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarbonitrile (101210-31-5) → 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni (101210-32-6)

Guidance literature:

With tin(IV) chloride; In tetrahydrofuran; dichloromethane; for 24h; Ambient temperature;

Reference yield:

5-Chloromethyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid tert-butyl ester (101210-29-1) → 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni (101210-32-6)

Guidance literature:

Multi-step reaction with 5 steps

1: Huenig's base

2: CF₃COOH

3: iodination

4: H₂, NaOAc / Pd-C

5: tin(IV) chloride / CH₂Cl₂

With hydrogen; sodium acetate; trifluoroacetic acid; palladium on activated charcoal; tin(IV) chloride; In dichloromethane;

DOI:10.1039/c39850001294

Reference yield:

1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methyloxycarbonylmethylpyrrol-2-yl>-3-<5-iodo-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>-2,2-dicyanopropane-2,2-dicarbonitrile (101210-50-8) → 1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<5-<5-formyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl>-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarboni (101210-32-6)

Guidance literature:

Multi-step reaction with 2 steps

1: H₂, NaOAc / Pd-C

2: tin(IV) chloride / CH₂Cl₂

With hydrogen; sodium acetate; palladium on activated charcoal; tin(IV) chloride; In dichloromethane;

DOI:10.1039/c39850001294

upstream raw materials:

3-(5-acetoxymethyl-2-formyl-4-methoxycarbonylmethyl-pyrrol-3-yl)-propionic acid methyl ester

1-<5-Benzyloxycarbonyl-3-(2-methoxycarbonylethyl)-4-methoxycarbonylmethylpyrrol-2-yl>-3-<4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-yl>propane-2,2-dicarbonitrile

5-Chloromethyl-3-(2-methoxycarbonyl-ethyl)-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid tert-butyl ester

5-chloromethyl-4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-pyrrole-2-carboxylic acid benzyl ester

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