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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 505499Generated: October 26, 2026

Water → {1-(4-Methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methanol

https://huagongshe.com/reaction/505499

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
Reactanttert-Butyl 1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridine-3-carboxylateHCID 56834061—
SolventTetrahydrofuranHCID 8028—
Product{1-(4-Methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridin-3-yl}methanolHCID 56833645—

Reaction Steps

To a solution of tert-butyl 1-(4-methoxybenzyl)-6-[(4-methoxybenzyl)amino]-1H-pyrazolo[3,4-b]pyridine-3-carboxylate (2.65 g, 5.58 mmol) in 30 mL THF cooled in an ice bath was added a 2M solution of LiAlH4 in THF (3.49 mL, 6.98 mmol). The resulting mixture was stirred cold for 20 minutes and then warmed to room temperature and then left at room temperature for 2.5 hours. The mixture was then diluted with THF (50 mL) and then treated sequentially with water (265 μL), 15% NaOH (265 μL) and water (795 μL) and then stirred for 30 minutes. The resulting suspension was filtered through diatomaceous earth and the resulting cake was rinsed with THF (50 mL). The combined filtrates were preabsorbed onto silica gel (15) and the solvent removed in vacuo. This solid was purified on silica gel (80 g) column (0-20% MeOH/CH2Cl2) to give the title compound. LRMS (M+1)=404.9

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07781454B2
Source datasetuspto-grants-2010_08
ORD IDord-4b855b13e6e2413ba08d6188d5b46a30
Source noteuspto-grants-2010_08