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

Base Information

Chemical Name:ethyl 6-ethyl-1-methyl-4-oxo-5-phenyl-3-(2,2,2-trifluoroethoxy)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate
CAS No.:1268523-36-9
Molecular Formula:C₂₁H₂₁F₃N₂O₄
Molecular Weight:422.404
Hs Code.:

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

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

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

There total 9 articles about ethyl 6-ethyl-1-methyl-4-oxo-5-phenyl-3-(2,2,2-trifluoroethoxy)-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: 97.0%

: 6226-25-1
2,2,2-trifluoroethyl trifluoromethanesulphonate

: 1268523-35-8
ethyl 6-ethyl-3-hydroxy-1-methyl-4-oxo-5-phenyl-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

: 1268523-36-9
ethyl 6-ethyl-1-methyl-4-oxo-5-phenyl-3-(2,2,2-trifluoroethoxy)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 2h;

Reference yield:

: 30414-53-0
methyl propanoyl acetate

: 1268523-36-9
ethyl 6-ethyl-1-methyl-4-oxo-5-phenyl-3-(2,2,2-trifluoroethoxy)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 8 steps

1: toluene-4-sulfonic acid / cyclohexane / 2 h / Reflux

2: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 7 h / 20 °C

3: triethylamine / tetrahydrofuran / 4 h / 20 °C

4: ethanol / 3 h / 50 °C

5: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / 1 h / Reflux

6: trichlorophosphate / acetonitrile / 2 h / Reflux

7: triethylamine / ethanol / 40 h / Reflux

8: caesium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogen; caesium carbonate; toluene-4-sulfonic acid; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; cyclohexane; N,N-dimethyl-formamide; toluene; acetonitrile;

Reference yield:

: 109245-01-4
methyl 3-(phenylamino)-2-pentenoate

: 1268523-36-9
ethyl 6-ethyl-1-methyl-4-oxo-5-phenyl-3-(2,2,2-trifluoroethoxy)-4,5-dihydro-1H-pyrrolo[3,2-c]pyridine-2-carboxylate

Guidance literature:: Multi-step reaction with 7 steps

1: hydrogen / palladium 10% on activated carbon / tetrahydrofuran / 7 h / 20 °C

2: triethylamine / tetrahydrofuran / 4 h / 20 °C

3: ethanol / 3 h / 50 °C

4: 2,3-dicyano-5,6-dichloro-p-benzoquinone / toluene / 1 h / Reflux

5: trichlorophosphate / acetonitrile / 2 h / Reflux

6: triethylamine / ethanol / 40 h / Reflux

7: caesium carbonate / N,N-dimethyl-formamide / 2 h / 20 °C

With hydrogen; caesium carbonate; triethylamine; 2,3-dicyano-5,6-dichloro-p-benzoquinone; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene; acetonitrile;