4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

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Chemical Name:4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile
CAS No.:1093101-62-2
Molecular Formula:C₃₄H₂₆N₁₀O
Molecular Weight:590.647
Hs Code.:

Synonyms:4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

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Chemical Property of 4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

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Technology Process of 4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

There total 7 articles about 4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile 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:

: 1093101-48-4
4-(8-amino-7-methylquinazolin-4-ylamino)benzonitrile

: 1093101-73-5
1-(4-methoxybenzyl)-4-(2-fluoropyridin-3-yl)-1H-pyrazolo[3,4-d]pyrimidine

: 1093101-62-2
4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

Guidance literature:: With lithium hexamethyldisilazane; In tetrahydrofuran; at 20 - 60 ℃; for 4.33333h; microwave;

Reference yield:

: 75844-40-5
7-methyl-quinazolin-4(3H)-one

: 1093101-62-2
4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

Guidance literature:: Multi-step reaction with 6 steps

1.1: methanol; acetic acid / 0.08 h / 20 °C

1.2: 3 h / 20 °C

2.1: sulfuric acid; nitric acid / 5.17 h / 0 - 20 °C

3.1: trichlorophosphate / 4 h / 130 °C

4.1: toluene / Heating / reflux

4.2: 5 h / Heating / reflux

5.1: hydrogen / palladium 10% on activated carbon / ethanol / 760.05 Torr

6.1: lithium hexamethyldisilazane / tetrahydrofuran / 4.33 h / 20 - 60 °C / microwave

With methanol; sulfuric acid; hydrogen; nitric acid; acetic acid; lithium hexamethyldisilazane; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; toluene;

Reference yield:

: 943605-85-4
6-bromo-7-methylquinazolin-4(3H)-one

: 1093101-62-2
4-(8-(3-(1-(4-methoxybenzyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-7-methylquinazolin-4-ylamino)benzonitrile

Guidance literature:: Multi-step reaction with 5 steps

1.1: sulfuric acid; nitric acid / 5.17 h / 0 - 20 °C

2.1: trichlorophosphate / 4 h / 130 °C

3.1: toluene / Heating / reflux

3.2: 5 h / Heating / reflux

4.1: hydrogen / palladium 10% on activated carbon / ethanol / 760.05 Torr

5.1: lithium hexamethyldisilazane / tetrahydrofuran / 4.33 h / 20 - 60 °C / microwave

With sulfuric acid; hydrogen; nitric acid; lithium hexamethyldisilazane; trichlorophosphate; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; toluene;