2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

Base Information

Chemical Name:2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone
CAS No.:130497-42-6
Molecular Formula:C₁₈H₂₅FN₂O
Molecular Weight:304.408
Hs Code.:

Synonyms:2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

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Chemical Property of 2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

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Technology Process of 2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

There total 4 articles about 2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone 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:

: 100158-63-2
2-[(1-Pyrrolidinyl)methyl]piperidine

: 459-04-1
4-Fluorophenylacetyl chloride

: 130497-42-6
2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

Guidance literature:: With potassium carbonate; In dichloromethane; at 0 ℃; for 3h;
DOI:10.1021/jm00105a061

Reference yield:

: 130605-98-0
1-(2-piperidinylcarbonyl)pyrrolidine

: 130497-42-6
2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / LiAlH₄ / tetrahydrofuran / 3 h / 30 °C

2: K₂CO₃ / CH₂Cl₂ / 3 h / 0 °C

With lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00105a061

Reference yield:

: 130497-14-2
(+/-)-[(N-ethoxycarbonyl)piperidine]-2-carboxylic acid

: 130497-42-6
2-(4-Fluoro-phenyl)-1-(2-pyrrolidin-1-ylmethyl-piperidin-1-yl)-ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: SOCl₂ / CH₂Cl₂ / 24 h / Ambient temperature

2: CH₂Cl₂ / -5 °C

3: 71 percent / LiAlH₄ / tetrahydrofuran / 3 h / 30 °C

4: K₂CO₃ / CH₂Cl₂ / 3 h / 0 °C

With lithium aluminium tetrahydride; thionyl chloride; potassium carbonate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00105a061