3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

Base Information

Chemical Name:3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine
CAS No.:1361570-74-2
Molecular Formula:C₁₇H₁₀ClFN₆O₂
Molecular Weight:384.757
Hs Code.:

Synonyms:3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

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Chemical Property of 3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

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Technology Process of 3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

There total 1 articles about 3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine 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: 62.0%

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

: 1361570-74-2
3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

Guidance literature:: With trichlorophosphate; In sulfolane; at 120 ℃; for 1h;

Reference yield: 89.0%

: 20781-20-8
2,4-Dimethoxybenzylamine

: 1361570-74-2
3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

: 1361570-75-3
N-(2,4-dimethoxybenzyl)-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-5-nitropyrimidin-4-amine

Guidance literature:: With diisopropylamine; In 1,4-dioxane; at 85 ℃; for 1h;

Reference yield:

: 1361570-74-2
3-(4-chloro-5-nitropyrimidin-2-yl)-1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine

: 1361570-79-7
7-(cyclopropylmethyl)-9-(2,4-dimethoxybenzyl)-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridin-3-yl]-7,9-dihydro-8H-purin-8-one

Guidance literature:: Multi-step reaction with 4 steps

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

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

3: acetonitrile / 4 h / Reflux

4: caesium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C

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