ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

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Chemical Name:ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate
CAS No.:1443300-23-9
Molecular Formula:C₁₈H₂₃N₂O₁₀P
Molecular Weight:458.362
Hs Code.:

Synonyms:ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

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Chemical Property of ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

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Technology Process of ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

There total 13 articles about ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-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: 52.0%

: 1443300-51-3
ethyl 3-(benzyloxy)-4-(((bis(benzyloxy)phosphoryl)oxy)methoxy)-5-(dimethylcarbamoyl)-1-(4-methoxyphenyl)-1H-pyrrole-2-carboxylate

: 1443300-23-9
ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 40 ℃;

Reference yield:

: 104-94-9
4-methoxy-aniline

: 1443300-23-9
ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1: sodium acetate; sodium iodide / water / 3 h / 90 °C

2: water; sodium hydroxide / tetrahydrofuran; ethanol / 3 h / 40 °C

3: N-ethyl-N,N-diisopropylamine; HATU / acetonitrile / 1 h / 20 °C

4: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 60 °C

5: sodium ethanolate / ethanol / 1.5 h / 85 °C

6: potassium iodide; potassium carbonate / N,N-dimethyl-formamide / 24 h / 80 °C

7: potassium carbonate / N,N-dimethyl-formamide / 45 h / 0 - 20 °C

8: hydrogen; palladium 10% on activated carbon / methanol / 40 °C

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

Reference yield:

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

: 1443300-23-9
ethyl 5-(dimethylcarbamoyl)-3-hydroxy-1-(4-methoxyphenyl)-4-((phosphonooxy)methoxy)-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

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

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

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

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

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

6: potassium iodide; potassium carbonate / N,N-dimethyl-formamide / 24 h / 80 °C

7: potassium carbonate / N,N-dimethyl-formamide / 45 h / 0 - 20 °C

8: hydrogen; palladium 10% on activated carbon / methanol / 40 °C

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