2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

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Chemical Name:2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one
CAS No.:1361570-15-1
Molecular Formula:C₂₄H₂₃FN₈O₂
Molecular Weight:474.497
Hs Code.:

Synonyms:2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

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Chemical Property of 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

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Technology Process of 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

There total 6 articles about 2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one 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: 69.0%

: 1361570-82-2
9-(2,4-dimethoxybenzyl)-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

: 1361570-15-1
2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

Guidance literature:: With triethylsilane; trifluoroacetic acid; for 18h; Reflux;

Reference yield:

: 1361570-73-1
2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5-nitropyrimidin-4-ol

: 1361570-15-1
2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

Guidance literature:: Multi-step reaction with 6 steps

1: trichlorophosphate / sulfolane / 1 h / 120 °C

2: diisopropylamine / 1,4-dioxane / 1 h / 85 °C

3: pyridine; palladium 10% on activated carbon; hydrogen / 2 h / 20 °C

4: acetonitrile / 4 h / Reflux

5: caesium carbonate / N,N-dimethyl-formamide / 40 h / 20 - 100 °C

6: triethylsilane; trifluoroacetic acid / 18 h / Reflux

With pyridine; triethylsilane; palladium 10% on activated carbon; hydrogen; caesium carbonate; diisopropylamine; trifluoroacetic acid; trichlorophosphate; In 1,4-dioxane; sulfolane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1361570-77-5
9-(2,4-dimethoxybenzyl)-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7,9-dihydro-8H-purin-8-one

: 1361570-15-1
2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7-[2-(morpholin-4-yl)ethyl]-7,9-dihydro-8H-purin-8-one

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate / N,N-dimethyl-formamide / 40 h / 20 - 100 °C

2: triethylsilane; trifluoroacetic acid / 18 h / Reflux

With triethylsilane; caesium carbonate; trifluoroacetic acid; In N,N-dimethyl-formamide;