N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

Base Information

Chemical Name:N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide
CAS No.:1068436-67-8
Molecular Formula:C₂₀H₂₁F₄N₃O₃S
Molecular Weight:459.465
Hs Code.:

Synonyms:N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

Chemical Property:

Purity/Quality:

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Technology Process of N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

There total 4 articles about N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide 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:

: 1068436-69-0
C₁₂H₁₅F₃N₂O₂S*ClH

: 351-04-2
2-chloro-N-(4-fluorophenyl)acetamide

: 1068436-67-8
N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

Guidance literature:: With potassium carbonate; potassium iodide; In acetonitrile; at 40 ℃; for 48h;

Reference yield:

: 1068436-68-9
C₁₇H₂₃F₃N₂O₄S

: 1068436-67-8
N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C

2: potassium carbonate; potassium iodide / acetonitrile / 48 h / 40 °C

With hydrogenchloride; potassium carbonate; potassium iodide; In 1,4-dioxane; acetonitrile;

Reference yield:

: 73874-95-0
(piperidin-4-yl)carbamic acid tert-butyl ester

: 1068436-67-8
N-(4-fluorophenyl)-2-[1-(3-trifluoromethyl-benzenesulfonyl)-piperidin-4-ylamino]acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / 12 h / 0 - 20 °C

2: hydrogenchloride / 1,4-dioxane / 12 h / 20 °C

3: potassium carbonate; potassium iodide / acetonitrile / 48 h / 40 °C

With hydrogenchloride; potassium carbonate; triethylamine; potassium iodide; In 1,4-dioxane; acetonitrile;