1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

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Chemical Name:1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea
CAS No.:1299488-13-3
Molecular Formula:C₂₇H₃₂ClF₇N₄O₂
Molecular Weight:613.019
Hs Code.:

Synonyms:1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

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Chemical Property of 1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

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Technology Process of 1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

There total 8 articles about 1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)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:

: 1299488-19-9
2-(4-((4-(2-chloro-4-amino-5-fluorobenzyl)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

: 7693-46-1
4-Nitrophenyl chloroformate

: 811-93-8
1,1-dimethylethylenediamine

: 1299488-13-3
1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: 2-(4-((4-(2-chloro-4-amino-5-fluorobenzyl)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol; 4-Nitrophenyl chloroformate; In tetrahydrofuran; at 20 ℃; for 0.5h;

1,1-dimethylethylenediamine; In tetrahydrofuran; at 20 ℃;

Reference yield:

: 33406-96-1
2-chloro-5-fluorotoluene

: 1299488-13-3
1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: Multi-step reaction with 8 steps

1.1: nitric acid; sulfuric acid / 2 h / 0 °C / Inert atmosphere

2.1: N-Bromosuccinimide / dibenzoyl peroxide / chlorobenzene / 4 h / Reflux

3.1: 3 h / 140 °C

4.1: sodium hydride / tetrahydrofuran / 3.5 h / 20 °C / Cooling with ice

5.1: hydrogen / platinum(IV) oxide / ethanol / 0.75 h / 2250.23 Torr

6.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

7.1: potassium carbonate / acetonitrile / 2 h / 20 °C

8.1: tetrahydrofuran / 0.5 h / 20 °C

8.2: 20 °C

With N-Bromosuccinimide; sulfuric acid; hydrogen; nitric acid; sodium hydride; potassium carbonate; trifluoroacetic acid; platinum(IV) oxide; dibenzoyl peroxide; In tetrahydrofuran; ethanol; dichloromethane; chlorobenzene; acetonitrile;

Reference yield:

: 170098-88-1
1-chloro-4-fluoro-2-methyl-5-nitrobenzene

: 1299488-13-3
1-(2-amino-2-methylpropyl)-3-(5-chloro-2-fluoro-4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)urea

Guidance literature:: Multi-step reaction with 7 steps

1.1: N-Bromosuccinimide / dibenzoyl peroxide / chlorobenzene / 4 h / Reflux

2.1: 3 h / 140 °C

3.1: sodium hydride / tetrahydrofuran / 3.5 h / 20 °C / Cooling with ice

4.1: hydrogen / platinum(IV) oxide / ethanol / 0.75 h / 2250.23 Torr

5.1: trifluoroacetic acid / dichloromethane / 0.5 h / 20 °C

6.1: potassium carbonate / acetonitrile / 2 h / 20 °C

7.1: tetrahydrofuran / 0.5 h / 20 °C

7.2: 20 °C

With N-Bromosuccinimide; hydrogen; sodium hydride; potassium carbonate; trifluoroacetic acid; platinum(IV) oxide; dibenzoyl peroxide; In tetrahydrofuran; ethanol; dichloromethane; chlorobenzene; acetonitrile;