1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

Base Information

Chemical Name:1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea
CAS No.:1299487-60-7
Molecular Formula:C₂₈H₂₈F₆N₄O₂
Molecular Weight:566.546
Hs Code.:

Synonyms:1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

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Chemical Property of 1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

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Technology Process of 1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

There total 5 articles about 1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)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:

: 1299487-38-9
2-(4-((4-(4-aminobenzyl)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

: 20951-01-3
pyridin-4-yl-carbamic acid phenyl ester

: 1299487-60-7
1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

Guidance literature:: In 1,4-dioxane; at 130 ℃; for 0.25h; Microwave irradiation;

Reference yield:

: 2609-49-6
diethyl p-nitrobenzylphosphonate

: 1299487-60-7
1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran / 20 °C / Cooling with ice

2: trifluoroacetic acid / dichloromethane / 3 h

3: potassium carbonate / acetonitrile / 5 h

4: hydrogen / 5% Pd(II)/C(eggshell) / ethyl acetate / 2250.23 Torr

5: 1,4-dioxane / 0.25 h / 130 °C / Microwave irradiation

With hydrogen; sodium hydride; potassium carbonate; trifluoroacetic acid; 5% Pd(II)/C(eggshell); In tetrahydrofuran; 1,4-dioxane; dichloromethane; ethyl acetate; acetonitrile;

Reference yield:

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

: 1299487-60-7
1-(4-((1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)methyl)phenyl)-3-(pyridin-4-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / tetrahydrofuran / 20 °C / Cooling with ice

2: trifluoroacetic acid / dichloromethane / 3 h

3: potassium carbonate / acetonitrile / 5 h

4: hydrogen / 5% Pd(II)/C(eggshell) / ethyl acetate / 2250.23 Torr

5: 1,4-dioxane / 0.25 h / 130 °C / Microwave irradiation

With hydrogen; sodium hydride; potassium carbonate; trifluoroacetic acid; 5% Pd(II)/C(eggshell); In tetrahydrofuran; 1,4-dioxane; dichloromethane; ethyl acetate; acetonitrile;