6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

Base Information

Chemical Name:6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide
CAS No.:1396770-73-2
Molecular Formula:C₂₅H₂₈N₆O₂
Molecular Weight:444.536
Hs Code.:

Synonyms:6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

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Chemical Property of 6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

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Technology Process of 6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

There total 8 articles about 6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide 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:

: 1396780-81-6
C₃₀H₃₆N₆O₄

: 1396770-73-2
6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

Guidance literature:: With trifluoroacetic acid; In dichloromethane;

Reference yield:

: 6-hydroxy-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl ester

: 1396770-73-2
6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: phosphorus(V) oxybromide / acetonitrile / 6 h / Reflux

2.1: potassium carbonate / acetonitrile / 8 h / Reflux

3.1: sodium hydroxide; water / ethanol / 1 h / 60 °C

4.1: dimethyl sulfoxide / 0.25 h / 20 °C

5.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 0.17 h / Inert atmosphere

5.2: 1.17 h / 100 °C / Inert atmosphere

6.1: trifluoroacetic acid / dichloromethane

With water; potassium carbonate; trifluoroacetic acid; sodium hydroxide; phosphorus(V) oxybromide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; ethanol; dichloromethane; dimethyl sulfoxide; acetonitrile; 5.1: Suzuki Coupling;

Reference yield:

: 6-bromo-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl ester

: 1396770-73-2
6-(4-(aminomethyl)phenyl)-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl-1H-pyrazolo[3,4-b]pyridine-4-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium carbonate / acetonitrile / 8 h / Reflux

2.1: sodium hydroxide; water / ethanol / 1 h / 60 °C

3.1: dimethyl sulfoxide / 0.25 h / 20 °C

4.1: tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 0.17 h / Inert atmosphere

4.2: 1.17 h / 100 °C / Inert atmosphere

5.1: trifluoroacetic acid / dichloromethane

With water; potassium carbonate; trifluoroacetic acid; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; ethanol; dichloromethane; dimethyl sulfoxide; acetonitrile; 4.1: Suzuki Coupling;