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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537128Generated: October 30, 2026

Sodium Hydroxide → 1H-Pyrazolo(4,3-b)pyridine-6-carboxylic acid

https://huagongshe.com/reaction/537128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethyl 1H-pyrazolo[4,3-B]pyridine-6-carboxylateHCID 60144275—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product1H-Pyrazolo(4,3-b)pyridine-6-carboxylic acidHCID 6715133921%

Reaction Steps

To a solution of methyl 1H-pyrazolo[4,3-b]pyridine-6-carboxylate (3.52 g, 20 mmol) in methanol (250 mL) and water (190 mL) at 0° C. was added aqueous sodium hydroxide (2M, 64 mL, 128 mmol), dropwise. The suspension was then allowed to warm to ambient temperature and stirred for 18 hours. The methanol was then removed in vacuo and the aqueous mixture extracted with ethyl acetate (250 mL). The aqueous layer was acidified (to pH 5-6) with 2 N aqueous hydrochloric acid (70 mL). The cream solid which had precipitated out was then filtered off and dried in a desiccator to yield the title compound (0.675 g, 21%). 1HNMR (400 MHz, DMSO-d6, δ): 8.97 (s, 1H), 8.45 (s, 1H), 8.39 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859773B2
Source datasetuspto-grants-2014_10
ORD IDord-ebc4a87a46104a858e01d9862070f239
Source noteuspto-grants-2014_10