3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

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Chemical Name:3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide
CAS No.:1351089-14-9
Molecular Formula:C₁₆H₁₉BrN₆O₃S
Molecular Weight:455.335
Hs Code.:

Synonyms:3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

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Chemical Property of 3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

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Technology Process of 3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

There total 5 articles about 3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide 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: 6.36%

: 1351094-39-7
3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-4-fluoro-N-methylbenzenesulfonamide

: 78-92-2,15892-23-6
iso-butanol

: 1351089-14-9
3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

Guidance literature:: iso-butanol; With sodium hydride; In methylpyrrolyrrolidin-2-one; 1-; mineral oil; at 20 ℃; for 0.5h;

3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-4-fluoro-N-methylbenzenesulfonamide; at 20 - 110 ℃; for 20.5h;

Reference yield:

: 1493-27-2,127723-77-7
ortho-nitrofluorobenzene

: 1351089-14-9
3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: chlorosulfonic acid / 18 h / 100 °C

2.1: triethylamine / tetrahydrofuran / 1 h / -35 °C

3.1: hydrogen / palladium / tetrahydrofuran / 50 °C / Inert atmosphere

4.1: acetic acid / 1,4-dioxane / 18 h / 100 °C / Sealed tube

5.1: sodium hydride / mineral oil; methylpyrrolyrrolidin-2-one; 1- / 0.5 h / 20 °C

5.2: 20.5 h / 20 - 110 °C

With chlorosulfonic acid; hydrogen; sodium hydride; acetic acid; triethylamine; palladium; In tetrahydrofuran; 1,4-dioxane; methylpyrrolyrrolidin-2-one; 1-; mineral oil;

Reference yield:

: 6668-56-0
4-fluoro-3-nitrobenzene-1-sulfonyl chloride

: 1351089-14-9
3-[(3-bromo-1H-pyrazolo[3,4-d]pyrimidin-4-yl)amino]-N-methyl-4-[(1-methylpropyl)oxy]benzenesuIfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / tetrahydrofuran / 1 h / -35 °C

2.1: hydrogen / palladium / tetrahydrofuran / 50 °C / Inert atmosphere

3.1: acetic acid / 1,4-dioxane / 18 h / 100 °C / Sealed tube

4.1: sodium hydride / mineral oil; methylpyrrolyrrolidin-2-one; 1- / 0.5 h / 20 °C

4.2: 20.5 h / 20 - 110 °C

With hydrogen; sodium hydride; acetic acid; triethylamine; palladium; In tetrahydrofuran; 1,4-dioxane; methylpyrrolyrrolidin-2-one; 1-; mineral oil;