3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Chemical Name:3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine
CAS No.:1459258-15-1
Molecular Formula:C₂₄H₂₄ClN₅O₂
Molecular Weight:449.94
Hs Code.:

Synonyms:3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Chemical Property of 3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

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Technology Process of 3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

There total 5 articles about 3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-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: 52.0%

: 1459257-91-0
1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-3-(trimethylstannyl)-1H-pyrazolo[4,3-c]pyridin-4-amine

: 22918-01-0
2-bromo-4-chloropyridine

: 1459258-15-1
3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: With copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; lithium chloride; In tetrahydrofuran; at 100 ℃; for 1h; Inert atmosphere; Microwave irradiation;

Reference yield:

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

: 1459258-15-1
3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

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

2: N-ethyl-N,N-diisopropylamine / butan-1-ol / 4 h / 180 °C

3: trans-bis(triphenylphosphine)palladium dichloride / toluene / 1 h / 140 °C / Inert atmosphere

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

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

Reference yield:

: 824-94-2
p-methoxybenzyl chloride

: 1459258-15-1
3-(4-chloropyridin-2-yl)-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 4 steps

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

2: N-ethyl-N,N-diisopropylamine / butan-1-ol / 4 h / 180 °C

3: trans-bis(triphenylphosphine)palladium dichloride / toluene / 1 h / 140 °C / Inert atmosphere

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

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