1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

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Chemical Name:1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea
CAS No.:1299488-10-0
Molecular Formula:C₃₀H₃₉F₇N₄O₂
Molecular Weight:620.654
Hs Code.:

Synonyms:1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

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Chemical Property of 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

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Technology Process of 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

There total 9 articles about 1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea 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:

: 1196694-62-8
1,1,1,3,3,3-hexafluoro-2-(4-(hydroxymethyl)-3-propylphenyl)propan-2-ol

: 1299488-12-2
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea

: 1299488-10-0
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: 1,1,1,3,3,3-hexafluoro-2-(4-(hydroxymethyl)-3-propylphenyl)propan-2-ol; With triethylamine; In dichloromethane;

With methanesulfonyl chloride; In dichloromethane; at 0 ℃; for 1.5h;

1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-(piperidin-4-ylmethyl)phenyl)urea; With potassium carbonate; In acetonitrile; for 16h; Reflux;

Reference yield:

: 131858-37-2
4-(bromomethyl)-2-fluoro-1-nitrobenzene

: 1299488-10-0
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: Multi-step reaction with 6 steps

1.1: 4 h / 140 °C

2.1: sodium hydride / tetrahydrofuran; oil / 4 h

3.1: potassium fluoride / palladium diacetate / tetrahydrofuran / 1 h / 20 °C / Sealed tube; Inert atmosphere

4.1: tetrahydrofuran / 1 h / 20 °C

4.2: 20 °C

5.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

6.1: triethylamine / dichloromethane

6.2: 1.5 h / 0 °C

6.3: 16 h / Reflux

With potassium fluoride; sodium hydride; triethylamine; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; dichloromethane; oil;

Reference yield:

: 1132941-95-7
3-fluoro-4-nitrobenzyl phosphonate

: 1299488-10-0
1-(2-amino-2-methylpropyl)-3-(2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)-2-propylbenzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydride / tetrahydrofuran; oil / 4 h

2.1: potassium fluoride / palladium diacetate / tetrahydrofuran / 1 h / 20 °C / Sealed tube; Inert atmosphere

3.1: tetrahydrofuran / 1 h / 20 °C

3.2: 20 °C

4.1: trifluoroacetic acid / dichloromethane / 3 h / 20 °C

5.1: triethylamine / dichloromethane

5.2: 1.5 h / 0 °C

5.3: 16 h / Reflux

With potassium fluoride; sodium hydride; triethylamine; trifluoroacetic acid; palladium diacetate; In tetrahydrofuran; dichloromethane; oil;