3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

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Chemical Name:3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid
CAS No.:1179343-99-7
Molecular Formula:C₂₉H₃₇N₅O₅
Molecular Weight:535.643
Hs Code.:

Synonyms:3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

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Chemical Property of 3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

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Technology Process of 3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

There total 9 articles about 3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid 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: 90.0%

: 1179344-00-3
methyl 3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoate

: 1179343-99-7
3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

Guidance literature:: methyl 3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoate; With lithium hydroxide monohydrate; water; In methanol; at 60 ℃; for 0.5h; Microwave irradiation;

With acetic acid; In methanol;

Reference yield:

: 1877-71-0
benzene 1,3-dicarboxylic acid monomethyl ester

: 1179343-99-7
3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

Guidance literature:: Multi-step reaction with 3 steps

1.1: chloroformic acid ethyl ester; triethylamine / dichloromethane / 0.17 h / 0 °C

1.2: 16 h / 20 °C

2.1: N,N-dimethyl-formamide / 44 h / 20 °C

2.2: 4 h / 20 °C

3.1: lithium hydroxide monohydrate; water / methanol / 0.5 h / 60 °C / Microwave irradiation

With lithium hydroxide monohydrate; water; chloroformic acid ethyl ester; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 21633-77-2
diethyl 2-propionylmalonate

: 1179343-99-7
3-{[4-({[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}oxy)-1-piperidinyl]carbonyl}benzoic acid

Guidance literature:: Multi-step reaction with 7 steps

1.1: tributyl-amine; trichlorophosphate / 22 h / 20 - 115 °C

2.1: triethylamine / toluene / 6 h / Reflux

2.2: 17.5 h / 110 °C

3.1: 1-Methylpyrrolidine; N-ethyl-N,N-diisopropylamine / 16 h / Reflux

4.1: methanol; lithium borohydride / tetrahydrofuran / 2.5 h / Reflux

5.1: thionyl chloride / 0.5 h / 20 °C

6.1: N,N-dimethyl-formamide / 44 h / 20 °C

6.2: 4 h / 20 °C

7.1: lithium hydroxide monohydrate; water / methanol / 0.5 h / 60 °C / Microwave irradiation

With 1-Methylpyrrolidine; methanol; lithium borohydride; thionyl chloride; lithium hydroxide monohydrate; tributyl-amine; water; triethylamine; N-ethyl-N,N-diisopropylamine; trichlorophosphate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide; toluene;