N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Chemical Name:N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine
CAS No.:1459258-28-6
Molecular Formula:C₂₄H₂₄F₂N₆O
Molecular Weight:450.491
Hs Code.:

Synonyms:N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Chemical Property of N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Technology Process of N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

There total 6 articles about N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-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: 88.0%

: 1459258-27-5
3-(6-chloropyrimidin-4-yl)-N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-1H-pyrazolo[4,3-c]pyridin-4-amine

: 1459258-28-6
N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: With palladium on activated charcoal; hydrogen; In methanol; at 50 ℃; for 10h;

Reference yield:

: 1186647-69-7
4-chloro-3-iodo-1H-pyrazolo[4,3-c]pyridine

: 1459258-28-6
N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hydroxide / N,N-dimethyl-formamide / 20 °C

2: N-ethyl-N,N-diisopropylamine / butan-1-ol / 2 h / 170 °C / Microwave irradiation

3: trans-bis(triphenylphosphine)palladium dichloride / toluene / 15 h / 110 °C / Inert atmosphere

4: lithium chloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 1 h / 100 °C / Inert atmosphere; Microwave irradiation

5: palladium on activated charcoal; hydrogen / methanol / 10 h / 50 °C

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trans-bis(triphenylphosphine)palladium dichloride; palladium on activated charcoal; hydrogen; N-ethyl-N,N-diisopropylamine; lithium chloride; potassium hydroxide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene; butan-1-ol;

Reference yield:

: 1459258-23-1
N-(4,4-difluorocyclohexyl)-3-iodo-1-(4-methoxybenzyl)-1H-pyrazolo[4,3-c]pyridin-4-amine

: 1459258-28-6
N-(4,4-difluorocyclohexyl)-1-(4-methoxybenzyl)-3-(pyrimidin-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 3 steps

1: trans-bis(triphenylphosphine)palladium dichloride / toluene / 15 h / 110 °C / Inert atmosphere

2: lithium chloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾ / tetrahydrofuran / 1 h / 100 °C / Inert atmosphere; Microwave irradiation

3: palladium on activated charcoal; hydrogen / methanol / 10 h / 50 °C

With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; trans-bis(triphenylphosphine)palladium dichloride; palladium on activated charcoal; hydrogen; lithium chloride; In tetrahydrofuran; methanol; toluene;