6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Base Information

Chemical Name:6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine
CAS No.:1361960-67-9
Molecular Formula:C₂₀H₂₀FN₇O₃S
Molecular Weight:457.488
Hs Code.:

Synonyms:6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

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Chemical Property of 6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

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Technology Process of 6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

There total 4 articles about 6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine 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: 18.0%

: 1361961-30-9
6-chloro-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

: 824-80-6
sodium 4-fluorobenzenesulfinate

: 1361960-67-9
6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: With 15-crown-5; In dimethyl sulfoxide; at 140 ℃; Sealed tube;

Reference yield:

: 1184920-55-5
4,6-dichloro-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidine

: 1361960-67-9
6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 2 steps

1: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 20 °C

2: 15-crown-5 / dimethyl sulfoxide / 140 °C / Sealed tube

With 15-crown-5; N-ethyl-N,N-diisopropylamine; potassium iodide; In dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 50270-27-4
2,4,6-trichloropyrimidine-5-carbaldehyde

: 1361960-67-9
6-(4-fluorophenylsulfonyl)-N-(5-methyl-1H-pyrazol-3-yl)-1-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / 3 h / -78 - 0 °C / Inert atmosphere

2: potassium iodide; N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 2 h / 20 °C

3: 15-crown-5 / dimethyl sulfoxide / 140 °C / Sealed tube

With 15-crown-5; triethylamine; N-ethyl-N,N-diisopropylamine; potassium iodide; In dimethyl sulfoxide; N,N-dimethyl-formamide;