N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

Base Information

Chemical Name:N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide
CAS No.:1240016-20-9
Molecular Formula:C₂₃H₂₂ClF₃N₂O
Molecular Weight:434.889
Hs Code.:

Synonyms:N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

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Chemical Property of N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

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Technology Process of N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

There total 6 articles about N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide 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:

: 657-05-6
2-chloro-5-trifluoromethylbenzoyl chloride

: 1244062-08-5
[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]amine

: 1240016-20-9
N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

Guidance literature:: With potassium carbonate; In dichloromethane; at 20 ℃;

Reference yield:

: 1240016-16-3
(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(morpholin-4-yl)methanone

: 1240016-20-9
N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: cyclohexane; diethyl ether; tetrahydrofuran / 1 h / -70 °C / Inert atmosphere

2.1: pyridine / Reflux

3.1: lithium aluminium tetrahydride / diethyl ether / 3 h / 40 °C / Inert atmosphere

3.2: double tartrate salt / 0 °C

4.1: potassium carbonate / dichloromethane / 20 °C

With pyridine; lithium aluminium tetrahydride; potassium carbonate; In tetrahydrofuran; diethyl ether; dichloromethane; cyclohexane;

Reference yield:

: 1240016-17-4
(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methanone

: 1240016-20-9
N-[(2-allyl-2-azabicyclo[2.1.1]hex-1-yl)(phenyl)methyl]-2-chloro-5-(trifluoro-methyl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: pyridine / Reflux

2.1: lithium aluminium tetrahydride / diethyl ether / 3 h / 40 °C / Inert atmosphere

2.2: double tartrate salt / 0 °C

3.1: potassium carbonate / dichloromethane / 20 °C

With pyridine; lithium aluminium tetrahydride; potassium carbonate; In diethyl ether; dichloromethane;