1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

Base Information

Chemical Name:1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine
CAS No.:1447121-59-6
Molecular Formula:C₂₂H₃₄N₄O₄S
Molecular Weight:450.602
Hs Code.:

Synonyms:1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

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Chemical Property of 1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

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Technology Process of 1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

There total 3 articles about 1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine 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:

: 14270-40-7
4-hydroxy-2-methyl(methylsulfonyl)benzene

: 1443288-43-4
(3-isopropyl-1,2,4-oxadiazol-5-yl)methyl bromide

: 1447123-00-3
tert-butyl 4-(methyl(2-(methylsulfonyloxy)ethyl)amino)piperidine-1-carboxylate

: 1447121-59-6
1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

Guidance literature:: 4-hydroxy-2-methyl(methylsulfonyl)benzene; tert-butyl 4-(methyl(2-(methylsulfonyloxy)ethyl)amino)piperidine-1-carboxylate; With sodium hydride; In acetone; Inert atmosphere; Reflux;

With trifluoroacetic acid; In ethyl acetate; for 0.5h; Reflux;

(3-isopropyl-1,2,4-oxadiazol-5-yl)methyl bromide; With caesium carbonate; In N,N-dimethyl-formamide; for 3h; Reflux;

Reference yield:

: 864655-25-4
tert-butyl 4-((2-hydroxyethyl)(methyl)amino)piperidine-1-carboxylate

: 1447121-59-6
1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1.1: triethylamine / chloroform / 0.5 h / 0 °C / Inert atmosphere

1.2: 3 h / 20 °C / Inert atmosphere

2.1: sodium hydride / acetone / Inert atmosphere; Reflux

2.2: 0.5 h / Reflux

2.3: 3 h / Reflux

With sodium hydride; triethylamine; In chloroform; acetone;

Reference yield:

: 79099-07-3
N-tert-butyloxycarbonylpiperidin-4-one

: 1447121-59-6
1-((3-isopropyl-1,2,4-oxadiazol-5-yl)methyl)-N-methyl-N-(2-(3-methyl-4-(methylsulfonyl)phenoxy)ethyl)piperidine-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1.1: acetic acid / tetrahydrofuran / 1 h / 0 - 20 °C / Inert atmosphere

1.2: 12 h / 20 °C

2.1: triethylamine / chloroform / 0.5 h / 0 °C / Inert atmosphere

2.2: 3 h / 20 °C / Inert atmosphere

3.1: sodium hydride / acetone / Inert atmosphere; Reflux

3.2: 0.5 h / Reflux

3.3: 3 h / Reflux

With sodium hydride; acetic acid; triethylamine; In tetrahydrofuran; chloroform; acetone;