N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

Base Information

Chemical Name:N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide
CAS No.:1352083-32-9
Molecular Formula:C₃₂H₃₀ClN₇O₂
Molecular Weight:580.089
Hs Code.:

Synonyms:N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

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Chemical Property of N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

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Technology Process of N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

There total 4 articles about N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide 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: 52.0%

: 1352083-31-8
{4-[(N-{[3-cyclohexyl-2-(pyridin-2-yl)-2H-indazol-6-yl]carbonyl}-D-alanyl)amino]phenyl}boronic acid

: 32779-36-5
5-Bromo-2-chloropyrimidine

: 1352083-32-9
N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

Guidance literature:: With potassium carbonate; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; at 90 ℃; for 2h; Inert atmosphere;

Reference yield:

: 1352083-30-7
N-{[3-cyclohexyl-2-(pyridin-2-yl)-2H-indazol-6-yl]carbonyl}-D-alanine

: 1352083-32-9
N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 18 h

2: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 2 h / 90 °C / Inert atmosphere

With potassium carbonate; N-ethyl-N,N-diisopropylamine; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; water; N,N-dimethyl-formamide;

Reference yield:

: 1352083-27-2
3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxylic acid

: 1352083-32-9
N-[(2R)-1-{[4-(2-chloropyrimidin-5-yl)phenyl]amino}-1-oxopropan-2-yl]-3-cyclohexyl-2-(pyridin-2-yl)-2H-indazole-6-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 17 h

2: potassium carbonate; water / ethanol / 1 h / 70 °C

3: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 18 h

4: potassium carbonate / dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂ / 1,4-dioxane; water / 2 h / 90 °C / Inert atmosphere

With water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH₂Cl₂; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;