3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

Base Information

Chemical Name:3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide
CAS No.:1310496-34-4
Molecular Formula:C₂₀H₂₃BrN₆O₂S
Molecular Weight:491.412
Hs Code.:

Synonyms:3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

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Chemical Property of 3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

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Technology Process of 3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

There total 3 articles about 3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide 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:

: 706820-95-3
N-(tert-butyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide

: 1266480-08-3
2,5-dibromo-N-(3-cyclopropyl-1H-pyrazol-5-yl)pyrimidin-4-amine

: 1310496-34-4
3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

Guidance literature:: With sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; at 100 ℃; for 3h; Inert atmosphere;

Reference yield:

: 308283-47-8
3-bromo-(N-tert-butyl)benzenesulfonamide

: 1310496-34-4
3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 2 h / 90 °C / Inert atmosphere

2: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 3 h / 100 °C / Inert atmosphere

With potassium acetate; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; 2: Suzuki Coupling;

Reference yield:

: 2905-24-0
3-Bromobenzenesulfonyl chloride

: 1310496-34-4
3-(4-(3-cyclopropyl-1H-pyrazol-5-ylamino)-5-bromopyrimidin-2-yl)-N-tert-butylbenzenesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1,4-dioxane / 1 h / 20 °C

2: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 2 h / 90 °C / Inert atmosphere

3: sodium carbonate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane; water / 3 h / 100 °C / Inert atmosphere

With potassium acetate; sodium carbonate; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In 1,4-dioxane; water; 3: Suzuki Coupling;