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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279100Generated: November 1, 2026

4-[4-(4-benzyl-2,2,5,5-tetramethyl-piperazin-1-ylmethyl)-3-methyl-1-(tetra-hydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-phenol → 4-[3-Methyl-1-(tetrahydro-pyran-2-yl)-4-(2,2,5,5-tetramethyl-piperazin-1-ylmethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-phenol

https://huagongshe.com/reaction/2279100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[4-(4-benzyl-2,2,5,5-tetramethyl-piperazin-1-ylmethyl)-3-methyl-1-(tetra-hydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-phenolHCID 136623189—
SolventMethanolHCID 887—
Product4-[3-Methyl-1-(tetrahydro-pyran-2-yl)-4-(2,2,5,5-tetramethyl-piperazin-1-ylmethyl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-phenolHCID 13662319172%

Reaction Steps

250 mg 4-[4-(4-benzyl-2,2,5,5-tetramethyl-piperazin-1-ylmethyl)-3-methyl-1-(tetra-hydro-pyran-2-yl)-1H-pyrazolo[3,4-b]pyridin-6-yl]-phenol was dissolved in 20 ml methanol and purged with argon. 25 mg Palladium (10% on charcoal) were added and the mixture was hydrogenated at r.t. for 30 min. The catalyst was filtered off and the solvents were evaporated. 150 mg (72%) of the title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133181B2
Source datasetuspto-grants-2015_09
ORD IDord-8ebeb12a1da947a49ce8ba0461e776d8
Source noteuspto-grants-2015_09