6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

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Chemical Name:6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide
CAS No.:1429171-63-0
Molecular Formula:C₃₂H₃₇N₅O₃
Molecular Weight:539.677
Hs Code.:

Synonyms:6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

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Chemical Property of 6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

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Technology Process of 6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

There total 5 articles about 6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide 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: 43.0%

: 163271-06-5
4-amino-1-benzyl-4-methylpiperidine

: 1429171-62-9
6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid

: 1429171-63-0
6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

Guidance literature:: With 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In 1,2-dichloro-ethane; at 20 - 40 ℃;

Reference yield:

: 123-08-0,65581-83-1
4-hydroxy-benzaldehyde

: 1429171-63-0
6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / methanol / 15 h / 75 °C

2.1: toluene-4-sulfonic acid / tetrahydrofuran / 20 °C

3.1: sodium hydroxide; water / isopropyl alcohol / 1.5 h / 20 °C

4.1: 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 20 - 40 °C

4.2: 0.5 h

With water; 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; toluene-4-sulfonic acid; acetic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; methanol; 1,2-dichloro-ethane; isopropyl alcohol;

Reference yield:

: 1429171-60-7
6-(4-hydroxyphenyl)-3-methyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid methyl ester

: 1429171-63-0
6-(4-hydroxyphenyl)-3-methyl-1-(tetrahydropyran-2-yl)-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid (1-benzyl-4-methylpiperidin-4-yl)amide

Guidance literature:: Multi-step reaction with 3 steps

1.1: toluene-4-sulfonic acid / tetrahydrofuran / 20 °C

2.1: sodium hydroxide; water / isopropyl alcohol / 1.5 h / 20 °C

3.1: 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; N-ethyl-N,N-diisopropylamine / 1,2-dichloro-ethane / 20 - 40 °C

3.2: 0.5 h

With water; 2-bromo-1-ethylpyridin-1-ium tetrafluoroborate; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; sodium hydroxide; In tetrahydrofuran; 1,2-dichloro-ethane; isopropyl alcohol;