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

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Chemical Name: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
CAS No.:1179344-00-3
Molecular Formula:C₃₀H₃₉N₅O₅
Molecular Weight:549.67
Hs Code.:

Synonyms: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

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Chemical Property of 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

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Technology Process of 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

There total 8 articles about 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 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: 36.0%

: 932113-90-1
5-(chloromethyl)-1,6-diethyl-4-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine-4-amine

: 1177559-57-7
Methyl 3-[(4-hydroxy-1-piperidinyl)carbonyl]benzoate

: 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

Guidance literature:: 5-(chloromethyl)-1,6-diethyl-4-(tetrahydro-2H-pyran-4-yl)-1H-pyrazolo[3,4-b]pyridine-4-amine; Methyl 3-[(4-hydroxy-1-piperidinyl)carbonyl]benzoate; In N,N-dimethyl-formamide; at 20 ℃; for 44h;

With triethylamine; In N,N-dimethyl-formamide; at 20 ℃; for 4h;

Reference yield:

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

: 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

Guidance literature:: Multi-step reaction with 2 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

With chloroformic acid ethyl ester; triethylamine; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 21633-77-2
diethyl 2-propionylmalonate

: 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

Guidance literature:: Multi-step reaction with 6 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

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