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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218467Generated: October 30, 2026

Sodium Hydroxide → 1H-Pyrazolo[4,3-b]pyridine-5-methanol

https://huagongshe.com/reaction/218467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantMethyl 1H-pyrazolo[4,3-b]pyridine-5-carboxylateHCID 59763244—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1H-Pyrazolo[4,3-b]pyridine-5-methanolHCID 5976328476.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

1H-pyrazolo[4,3-b]pyridine-5-carboxylic acid, methyl ester (420 mg, 2.37 mmol) was dissolved in THF (30 mL) and cooled to 0° C. LiAlH4 (360 mg, 9.48 mmol) was added in one portion. The mixture was stirred at 0° C. for 3 hr, and diluted with ether. 50% NaOH (5 mL) was added to quench the reaction, and the solid was filtered off through Celite. The filtrate was concentrated, and the residue was purified by flash chromatography to afford 1H-pyrazolo[4,3-b]pyridine-5-methanol (270 mg, 76.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198456B2
Source datasetuspto-grants-2012_06
ORD IDord-a3d0eb9f03954c208ff630209fd87fa3
Source noteuspto-grants-2012_06