5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

Base Information

Chemical Name:5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline
CAS No.:1253734-01-8
Molecular Formula:C₃₀H₃₇F₂N₅O₃SSi
Molecular Weight:613.804
Hs Code.:

Synonyms:5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

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Chemical Property of 5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

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Technology Process of 5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

There total 4 articles about 5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline 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:

: 18063-02-0
2,6-difluorobenzoylchloride

: 1253734-01-8
5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / ethanol; water; tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

1.2: 20 °C

2.1: phosphorus pentoxide / 23 h / 165 °C / Inert atmosphere

3.1: potassium hydroxide; bromine / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: 0.17 h / Inert atmosphere

4.2: 1 h / 100 °C

4.3: 0.5 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

6.1: 1,4-dioxane / 0.17 h / Inert atmosphere

6.2: 4 h / Reflux

With phosphorus pentoxide; bromine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1253733-68-4
3-(4-iodophenyl)-1H-pyrazol-4-ylamine

: 1253734-01-8
5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / ethanol; water; tetrahydrofuran / 1 h / 20 °C / Inert atmosphere

1.2: 20 °C

2.1: phosphorus pentoxide / 23 h / 165 °C / Inert atmosphere

3.1: potassium hydroxide; bromine / N,N-dimethyl-formamide / 1 h / 20 °C

4.1: 0.17 h / Inert atmosphere

4.2: 1 h / 100 °C

4.3: 0.5 h / 20 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

6.1: 1,4-dioxane / 0.17 h / Inert atmosphere

6.2: 4 h / Reflux

With phosphorus pentoxide; bromine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;

Reference yield:

: 1253733-71-9
5-(2,6-difluorophenyl)-7-iodo-1H-pyrazolo[4,3-c]isoquinoline

: 1253734-01-8
5-(2,6-difluorophenyl)-3-{[1-(methylsulphonyl)piperidin-4-yl]amino}-2-{[2-(trimethylsilyl)ethoxy]methyl}-7-vinyl-2H-pyrazolo[4,3-c]isoquinoline

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium hydroxide; bromine / N,N-dimethyl-formamide / 1 h / 20 °C

2.1: 0.17 h / Inert atmosphere

2.2: 1 h / 100 °C

2.3: 0.5 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere

4.1: 1,4-dioxane / 0.17 h / Inert atmosphere

4.2: 4 h / Reflux

With bromine; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In 1,4-dioxane; N,N-dimethyl-formamide;