(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

Base Information

Chemical Name:(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate
CAS No.:1580002-65-8
Molecular Formula:C₂₄H₂₈FN₃O₃
Molecular Weight:425.503
Hs Code.:

Synonyms:(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

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Chemical Property of (E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

Chemical Property:

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Technology Process of (E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

There total 5 articles about (E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-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: 70.15%

: 154590-35-9
tert-butyl 4-(4-amino-2-fluorophenyl)piperazine-1-carboxylate

: 102-92-1,17082-09-6
Cinnamoyl chloride

: 1580002-65-8
(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

Guidance literature:: With pyridine; In dichloromethane; at 0 ℃; for 3h; Inert atmosphere;
DOI:10.1016/j.ejmech.2014.01.024

Reference yield:

: 369-34-6
3,4-difluoronitrobenzene

: 1580002-65-8
(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dimethyl sulfoxide / 12 h / 90 °C

2: hydrogen; palladium 10% on activated carbon / ethyl acetate; methanol / 6 h / 5171.62 Torr

3: pyridine / dichloromethane / 3 h / 0 °C / Inert atmosphere

With pyridine; palladium 10% on activated carbon; hydrogen; potassium carbonate; In methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate;
DOI:10.1016/j.ejmech.2014.01.024

Reference yield:

: 57260-71-6
1-t-Butoxycarbonylpiperazine

: 1580002-65-8
(E)-tert-butyl 4-(4-cinnamamido-2-fluorophenyl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / dimethyl sulfoxide / 12 h / 90 °C

2: hydrogen; palladium 10% on activated carbon / ethyl acetate; methanol / 6 h / 5171.62 Torr

3: pyridine / dichloromethane / 3 h / 0 °C / Inert atmosphere

With pyridine; palladium 10% on activated carbon; hydrogen; potassium carbonate; In methanol; dichloromethane; dimethyl sulfoxide; ethyl acetate;
DOI:10.1016/j.ejmech.2014.01.024