ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

Base Information

Chemical Name:ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate
CAS No.:1296654-72-2
Molecular Formula:C₁₆H₁₅F₃N₂O₃
Molecular Weight:340.302
Hs Code.:

Synonyms:ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

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Chemical Property of ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

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Technology Process of ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

There total 6 articles about ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-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:

: 1296654-70-0
ethyl 1-amino-4-methyl-3-phenyl-1H-pyrrole-2-carboxylate

: 407-25-0
trifluoroacetic anhydride

: 1296654-72-2
ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 3154-51-6
ethyl N-formylglycinate

: 1296654-72-2
ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine; trichlorophosphate / dichloromethane / 1 h / -10 °C

2.1: potassium carbonate / tetrahydrofuran / 16 h / 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

3.2: 0.5 h

4.1: triethylamine / dichloromethane / 2 h / 20 °C

With sodium hydride; potassium carbonate; triethylamine; trichlorophosphate; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 100-52-7
benzaldehyde

: 1296654-72-2
ethyl 4-methyl-3-phenyl-1-[(trifluoroacetyl)amino]-1H-pyrrole-2-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: ammonium acetate; acetic acid / 5 h / Reflux

2.1: potassium carbonate / tetrahydrofuran / 16 h / 20 °C

3.1: sodium hydride / N,N-dimethyl-formamide / 1 h / 20 °C / Inert atmosphere

3.2: 0.5 h

4.1: triethylamine / dichloromethane / 2 h / 20 °C

With ammonium acetate; sodium hydride; potassium carbonate; acetic acid; triethylamine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;