N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

Base Information

Chemical Name:N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide
CAS No.:1395922-18-5
Molecular Formula:C₂₂H₃₁FN₂O₃
Molecular Weight:390.498
Hs Code.:

Synonyms:N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

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Chemical Property of N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

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Technology Process of N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

There total 7 articles about N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-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: 66.7%

: 453-18-9
methyl fluoroacetate

: trans-4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexylamine hydrochloride

: 1395922-18-5
N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

Guidance literature:: methyl fluoroacetate; With potassium trimethylsilonate; In 1,4-dioxane; at 20 ℃;

trans-4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexylamine hydrochloride; With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In 1,4-dioxane; at 20 ℃; for 4h;

Reference yield:

: 6698-13-1
4-bromo-benzo[1,3]dioxole

: 1395922-18-5
N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; sodium carbonate / palladium diacetate / 1,2-dimethoxyethane / 85 °C / Inert atmosphere

2.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C

3.1: ammonium formate / palladium 10% on activated carbon / methanol / 1 h / Inert atmosphere; Reflux

4.1: dichloromethane; methanol / 2 h / 20 °C

4.2: 16 h / 20 °C

5.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C

6.1: potassium trimethylsilonate / 1,4-dioxane / 20 °C

6.2: 4 h / 20 °C

With hydrogenchloride; potassium trimethylsilonate; ammonium formate; sodium carbonate; triphenylphosphine; palladium 10% on activated carbon; palladium diacetate; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane;

Reference yield:

: 375853-82-0,286961-14-6
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,6-dihydro-1(2H)-pyridinecarboxylate

: 1395922-18-5
N-trans-{4-[2-(4-benzo[1,3]dioxol-4-yl-piperidin-1-yl)-ethyl]-cyclohexyl}-2-fluoro-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: triphenylphosphine; sodium carbonate / palladium diacetate / 1,2-dimethoxyethane / 85 °C / Inert atmosphere

2.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C

3.1: ammonium formate / palladium 10% on activated carbon / methanol / 1 h / Inert atmosphere; Reflux

4.1: dichloromethane; methanol / 2 h / 20 °C

4.2: 16 h / 20 °C

5.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 4 h / 20 °C

6.1: potassium trimethylsilonate / 1,4-dioxane / 20 °C

6.2: 4 h / 20 °C

With hydrogenchloride; potassium trimethylsilonate; ammonium formate; sodium carbonate; triphenylphosphine; palladium 10% on activated carbon; palladium diacetate; In 1,4-dioxane; methanol; 1,2-dimethoxyethane; dichloromethane;