ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

Base Information

Chemical Name:ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate
CAS No.:1443053-33-5
Molecular Formula:C₂₃H₃₀N₄O₈
Molecular Weight:490.513
Hs Code.:

Synonyms:ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

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Chemical Property of ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

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Technology Process of ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

There total 11 articles about ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate 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: 14.0%

: 1443052-79-6
ethyl 5-(dimethylcarbamoyl)-3,4-dihydroxy-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

: 79-44-7
N,N-Dimethylcarbamoyl chloride

: 1443053-33-5
ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 16h;

Reference yield:

: 98269-30-8
diethyl 2,2’-((4-methoxyphenyl)azanediyl)diacetate

: 1443053-33-5
ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: sodium ethanolate / ethanol / 1 h / 100 °C

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 60 °C

3: sodium hydroxide; water / tetrahydrofuran; ethanol / 16 h / 50 °C

4: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

5: palladium 10% on activated carbon; hydrogen / ethanol / 1.5 h / 20 °C / Inert atmosphere

6: potassium carbonate / acetonitrile / 16 h / 80 °C

With palladium 10% on activated carbon; water; hydrogen; sodium ethanolate; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; sodium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1443053-94-8
triethylammonium 3,4-bis(benzyloxy)-5-(ethoxycarbonyl)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

: 1443053-33-5
ethyl 5-(dimethylcarbamoyl)-3,4-bis((dimethylcarbamoyl)oxy)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 16 h / 0 - 20 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 1.5 h / 20 °C / Inert atmosphere

3: potassium carbonate / acetonitrile / 16 h / 80 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; In ethanol; N,N-dimethyl-formamide; acetonitrile;