N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

Base Information

Chemical Name:N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide
CAS No.:684213-06-7
Molecular Formula:C₂₉H₃₇FN₄O
Molecular Weight:476.637
Hs Code.:

Synonyms:N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

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Chemical Property of N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

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Technology Process of N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

There total 11 articles about N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide 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: 35.7%

: N-cyclohexyl-N-phenyl-2-(piperazin-1-yl)-acetamide Trifluoroacetate

: 191013-68-0
3-(3-Bromopropyl)-5-fluoro-1H-indole

: 684213-06-7
N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 85 ℃; for 12h;
DOI:10.1021/acs.jcim.9b00926

Reference yield: 35.7%

: 1452807-01-0
N-cyclohexyl-N-phenyl-2-(piperazin-1-yl)acetamide

: 191013-68-0
3-(3-Bromopropyl)-5-fluoro-1H-indole

: 684213-06-7
N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 12h;
DOI:10.1111/cbdd.12158

Reference yield:

: 1452806-97-1
tert-butyl 4-(2-(cyclohexyl(phenyl)amino)-2-oxoethyl)piperazine-1-carboxylate

: 684213-06-7
N-cyclohexyl-2-(4-(3-(5-fluoro-1H-indol-3-yl)propyl)piperazin-1-yl)-N-phenylacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 12 h / 20 °C

2: potassium carbonate / acetonitrile / 12 h / 80 °C

With potassium carbonate; trifluoroacetic acid; In dichloromethane; acetonitrile;
DOI:10.1111/cbdd.12158