ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

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Chemical Name:ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
CAS No.:1186188-60-2
Molecular Formula:C₂₃H₂₆N₂O₅
Molecular Weight:410.47
Hs Code.:

Synonyms:ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

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Chemical Property of ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

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Technology Process of ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

There total 5 articles about ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-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: 82.0%

: 64-67-5
diethyl sulfate

: 1186188-53-3
ethyl 6-ethyl-3-hydroxy-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo-[3,2-c]pyridine-2-carboxylate

: 1186188-60-2
ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: With potassium carbonate; In acetone; for 18h; Reflux;
DOI:10.1016/j.bmc.2012.07.034

Reference yield:

: 30414-53-0
methyl propanoyl acetate

: 1186188-60-2
ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1: ammonium acetate / methanol / 72 h / 20 °C

2: sodium ethanolate / ethanol; 5,5-dimethyl-1,3-cyclohexadiene / 19 h / 120 - 150 °C

3: trichlorophosphate / 0.5 h / 80 °C

4: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

5: triethylamine / ethanol / 48 h / Reflux

6: potassium carbonate / acetone / 18 h / Reflux

With ammonium acetate; sodium ethanolate; potassium carbonate; triethylamine; trichlorophosphate; In methanol; 5,5-dimethyl-1,3-cyclohexadiene; ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmc.2012.07.034

Reference yield:

: 125604-20-8
ethyl 6-ethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate

: 1186188-60-2
ethyl 3-ethoxy-6-ethyl-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / 0.5 h / 80 °C

2: potassium carbonate / N,N-dimethyl-formamide / 15 h / 20 °C

3: triethylamine / ethanol / 48 h / Reflux

4: potassium carbonate / acetone / 18 h / Reflux

With potassium carbonate; triethylamine; trichlorophosphate; In ethanol; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.bmc.2012.07.034