(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

Base Information

Chemical Name:(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone
CAS No.:1361961-18-3
Molecular Formula:C₁₃H₈ClFN₄O
Molecular Weight:290.684
Hs Code.:

Synonyms:(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

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Technology Process of (4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

There total 4 articles about (4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone 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: 28.0%

: 1361961-17-2
ethyl 4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-carboxylate

: 352-13-6
4-flourophenylmagnesium bromide

: 1361961-18-3
(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

Guidance literature:: In tetrahydrofuran; at -30 ℃; for 1h; Inert atmosphere;

Reference yield:

: 21230-50-2
3-amino-1-methyl-1H-pyrazole-4-carbonitrile

: 1361961-18-3
(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1.1: sulfuric acid / 1 h / 0 - 20 °C

1.2: 0.17 h / 0 - 20 °C / pH 7 - 8

2.1: hydrogenchloride / water; acetic acid / 5 h / 100 °C

3.1: trichlorophosphate / 2 h / 85 °C

4.1: tetrahydrofuran / 1 h / -30 °C / Inert atmosphere

With hydrogenchloride; sulfuric acid; trichlorophosphate; In tetrahydrofuran; water; acetic acid;

Reference yield:

: 89181-79-3
3-amino-1-methyl-1H-pyrazole-4-carboxamide

: 1361961-18-3
(4-chloro-2-methyl-2H-pyrazolo[3,4-d]pyrimidin-6-yl)(4-fluorophenyl)methanone

Guidance literature:: Multi-step reaction with 3 steps

1: hydrogenchloride / water; acetic acid / 5 h / 100 °C

2: trichlorophosphate / 2 h / 85 °C

3: tetrahydrofuran / 1 h / -30 °C / Inert atmosphere

With hydrogenchloride; trichlorophosphate; In tetrahydrofuran; water; acetic acid;