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

Base Information

Chemical Name:(4-methoxybenzyl)-3-phenoxy-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine
CAS No.:1367875-50-0
Molecular Formula:C₂₅H₂₆N₄O₃
Molecular Weight:430.506
Hs Code.:

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

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

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

There total 6 articles about (4-methoxybenzyl)-3-phenoxy-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:

: 1367874-54-1
3-iodo-1-(4-methoxybenzyl)-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

: 108-95-2,27073-41-2
phenol

: 1367875-50-0
(4-methoxybenzyl)-3-phenoxy-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: With dimethylaminoacetic acid; caesium carbonate; copper(l) iodide; In 1,4-dioxane; at 120 ℃; for 24h; Inert atmosphere;

Reference yield:

: 134031-24-6
2,4-dichloro-3-pyridine Carboxaldehyde

: 1367875-50-0
(4-methoxybenzyl)-3-phenoxy-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 5 steps

1: hydrazine hydrate / 1,2-dimethoxyethane / 20 - 75 °C

2: iodine; potassium hydroxide / 1,4-dioxane / 4 h / 75 °C

3: potassium hydroxide / N,N-dimethyl-formamide / 2.5 h / 20 °C

4: butan-1-ol / 1 h / 20 - 180 °C / Microwave irradiation

5: dimethylaminoacetic acid; caesium carbonate / copper(l) iodide / 1,4-dioxane / 24 h / 120 °C / Inert atmosphere

With dimethylaminoacetic acid; iodine; caesium carbonate; hydrazine hydrate; potassium hydroxide; copper(l) iodide; In 1,4-dioxane; 1,2-dimethoxyethane; N,N-dimethyl-formamide; butan-1-ol;

Reference yield:

: 26452-80-2
2,4-dichloropyridine

: 1367875-50-0
(4-methoxybenzyl)-3-phenoxy-N-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[4,3-c]pyridin-4-amine

Guidance literature:: Multi-step reaction with 6 steps

1.1: n-butyllithium; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 3.5 h / -78 - 0 °C

1.2: 1.5 h / -78 °C

2.1: hydrazine hydrate / 1,2-dimethoxyethane / 20 - 75 °C

3.1: iodine; potassium hydroxide / 1,4-dioxane / 4 h / 75 °C

4.1: potassium hydroxide / N,N-dimethyl-formamide / 2.5 h / 20 °C

5.1: butan-1-ol / 1 h / 20 - 180 °C / Microwave irradiation

6.1: dimethylaminoacetic acid; caesium carbonate / copper(l) iodide / 1,4-dioxane / 24 h / 120 °C / Inert atmosphere

With n-butyllithium; dimethylaminoacetic acid; iodine; caesium carbonate; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; potassium hydroxide; copper(l) iodide; In tetrahydrofuran; 1,4-dioxane; 1,2-dimethoxyethane; N,N-dimethyl-formamide; butan-1-ol;