N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

Base Information

Chemical Name:N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide
CAS No.:1309785-50-9
Molecular Formula:C₂₀H₁₉N₅O₄S₂
Molecular Weight:457.534
Hs Code.:

Synonyms:N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

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Chemical Property of N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

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Technology Process of N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

There total 5 articles about N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide 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:

: 1093819-39-6
N-(5-bromo-2-methyl-pyridin-3-yl)-methanesulfonamide

: 1-(phenylsulfonyl)-6-(4,4,6,6-tetramethyl-1,3,2-dioxaborinan-2-yl)-1H-indazol-4-amine

: 1309785-50-9
N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

Guidance literature:: With potassium phosphate; 2’-(dimethylamino)-2-biphenylyl-palladium(II)chloride dinorbornylphosphine complex; In 1,4-dioxane; water; at 100 ℃; for 0.25h; microwave;

Reference yield:

: 98-09-9
benzenesulfonyl chloride

: 1309785-50-9
N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Cooling with ice

1.2: 0.25 h / 20 °C

1.3: 20 °C

2.1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 1 h / 80 °C / microwave vial

3.1: potassium phosphate / 2’-(dimethylamino)-2-biphenylyl-palladium(II)chloride dinorbornylphosphine complex / 1,4-dioxane; water / 0.25 h / 100 °C / microwave

With potassium phosphate; potassium acetate; sodium hydride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; 2’-(dimethylamino)-2-biphenylyl-palladium(II)chloride dinorbornylphosphine complex; In 1,4-dioxane; water; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 885518-50-3
6-bromo-1H-indazole-4-amine

: 1309785-50-9
N-{5-[4-amino-1-(phenylsulfonyl)-1H-indazol-6-yl]-2-methyl-3-pyridinyl}methanesulfonamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / Cooling with ice

1.2: 0.25 h / 20 °C

1.3: 20 °C

2.1: potassium acetate / (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride / 1,4-dioxane / 1 h / 80 °C / microwave vial

3.1: potassium phosphate / 2’-(dimethylamino)-2-biphenylyl-palladium(II)chloride dinorbornylphosphine complex / 1,4-dioxane; water / 0.25 h / 100 °C / microwave

With potassium phosphate; potassium acetate; sodium hydride; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; 2’-(dimethylamino)-2-biphenylyl-palladium(II)chloride dinorbornylphosphine complex; In 1,4-dioxane; water; N,N-dimethyl-formamide; mineral oil;