1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

Base Information

Chemical Name:1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea
CAS No.:1299488-97-3
Molecular Formula:C₂₈H₂₆F₆N₆O₂
Molecular Weight:592.544
Hs Code.:

Synonyms:1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

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Chemical Property of 1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

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Technology Process of 1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

There total 6 articles about 1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-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:

: 1299489-00-1
2-(4-((4-(5-amino-1H-indazol-1-yl)piperidin-1-yl)methyl)phenyl)-1,1,1,3,3,3-hexafluoropropan-2-ol

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

: 1299488-97-3
1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

Guidance literature:: In 1,4-dioxane; at 100 ℃;

Reference yield:

: 5401-94-5
5-nitroindazole

: 1299488-97-3
1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 3 h / 100 °C

2: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 3750.38 Torr

3: trifluoroacetic acid / dichloromethane / 1 h

4: potassium carbonate / acetonitrile / 72 h / 20 °C

5: 1,4-dioxane / 100 °C

With hydrogen; potassium carbonate; trifluoroacetic acid; palladium 10% on activated carbon; In 1,4-dioxane; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1203667-11-1
tert-butyl 4-(5-nitro-1H-indazol-1-yl)piperidine-1-carboxylate

: 1299488-97-3
1-(2-(1-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)piperidin-4-yl)-1H-indazol-5-yl)-3-(pyridin-4-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogen / palladium 10% on activated carbon / ethanol / 1 h / 3750.38 Torr

2: trifluoroacetic acid / dichloromethane / 1 h

3: potassium carbonate / acetonitrile / 72 h / 20 °C

4: 1,4-dioxane / 100 °C

With hydrogen; potassium carbonate; trifluoroacetic acid; palladium 10% on activated carbon; In 1,4-dioxane; ethanol; dichloromethane; acetonitrile;