2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

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Chemical Name:2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole
CAS No.:114091-95-1
Molecular Formula:C₃₂H₃₈N₂O₁₀
Molecular Weight:610.661
Hs Code.:

2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

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Chemical Property of 2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

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Technology Process of 2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

There total 10 articles about 2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole 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: 45.0%

: 114091-94-0
3-(2-Methoxycarbonyl-ethyl)-5-[4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-2-methyl-5-thioxo-2,5-dihydro-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

: 114091-95-1
2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

Guidance literature:: With nickel boride; In methanol; acetic acid;
DOI:10.1039/c39870001313

Reference yield: 5.0%

: 114091-94-0
3-(2-Methoxycarbonyl-ethyl)-5-[4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-2-methyl-5-thioxo-2,5-dihydro-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

: 114091-95-1
2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

: 207971-44-6
3-(2-Methoxycarbonyl-ethyl)-5-[4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-2-methyl-2,5-dihydro-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

Guidance literature:: With nickel boride; hydrogen; acetic acid; In methanol; for 0.5h; Ambient temperature;
DOI:10.1039/a708132d

Reference yield:

: 114091-93-9
3-(2-Methoxycarbonyl-ethyl)-5-[4-(2-methoxycarbonyl-ethyl)-3-methoxycarbonylmethyl-2-methyl-5-oxo-2,5-dihydro-1H-pyrrol-2-ylmethyl]-4-methoxycarbonylmethyl-1H-pyrrole-2-carboxylic acid benzyl ester

: 114091-95-1
2-[5-Benzyloxycarbonyl-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethylpyrrol-2-ylmethyl]-4-(2-methoxycarbonylethyl)-3-methoxycarbonylmethyl-2-methyl-2H-pyrrole

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / Lawesson's reagent / benzene / 0.75 h / Heating

2: 45 percent / nickel boride, acetic acid, H₂ / methanol / 0.5 h / Ambient temperature

With Lawessons reagent; nickel boride; hydrogen; acetic acid; In methanol; benzene;
DOI:10.1039/a708132d