3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

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Chemical Name:3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine
CAS No.:1415637-39-6
Molecular Formula:C₂₂H₂₂FN₇
Molecular Weight:403.462
Hs Code.:

Synonyms:3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

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Chemical Property of 3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

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Technology Process of 3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

There total 5 articles about 3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine 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: 49.0%

: 1124-14-7
1-bromo-4-cyclopropylbenzene

: 1415638-03-7
4-(3-fluoroazetidin-1-yl)-1-methyl-3-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidine

: 1415637-39-6
3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

Guidance literature:: With potassium carbonate; palladium diacetate; In 1,4-dioxane; at 100 ℃; for 48h;

Reference yield:

: 5334-56-5
4-hydroxy-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

: 1415637-39-6
3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

Guidance literature:: Multi-step reaction with 5 steps

1: tetrafluoroboric acid; N-iodo-succinimide / acetonitrile; water / 5 h / Reflux

2: trichlorophosphate / N,N-dimethyl-formamide; 1,2-dichloro-ethane / 2 h / 80 °C

3: sodium hydrogencarbonate / water; tetrahydrofuran / 18 h / 20 °C

4: tricyclohexylphosphine; potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane; water / 1.5 h / 150 °C

5: potassium carbonate / palladium diacetate / 1,4-dioxane / 48 h / 100 °C

With N-iodo-succinimide; tetrafluoroboric acid; potassium phosphate; sodium hydrogencarbonate; potassium carbonate; trichlorophosphate; tricyclohexylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In tetrahydrofuran; 1,4-dioxane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1415638-01-5
3-iodo-1-methyl-I H-pyrazolo[3,4-d]pyrimidin-4-ol

: 1415637-39-6
3-[5-(4-cyclopropylphenyl)-1-methyl-1H-pyrazol-4-yl]-4-(3-fluoroazetidin-1-yl)-1-methyl-1H-pyrazolo[3,4-d]pyrimidine

Guidance literature:: Multi-step reaction with 4 steps

1: trichlorophosphate / N,N-dimethyl-formamide; 1,2-dichloro-ethane / 2 h / 80 °C

2: sodium hydrogencarbonate / water; tetrahydrofuran / 18 h / 20 °C

3: tricyclohexylphosphine; potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,4-dioxane; water / 1.5 h / 150 °C

4: potassium carbonate / palladium diacetate / 1,4-dioxane / 48 h / 100 °C

With potassium phosphate; sodium hydrogencarbonate; potassium carbonate; trichlorophosphate; tricyclohexylphosphine; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium diacetate; In tetrahydrofuran; 1,4-dioxane; water; 1,2-dichloro-ethane; N,N-dimethyl-formamide;