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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393663Generated: November 1, 2026

Water → 2-(Hydroxymethyl)pyrazolo[1,5-A]pyrimidine-6-carboxylic acid

https://huagongshe.com/reaction/1393663

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(hydroxymethyl)pyrazolo[1,5-A]pyrimidine-6-carboxylateHCID 23091920—
SolventTetrahydrofuranHCID 8028—
Product2-(Hydroxymethyl)pyrazolo[1,5-A]pyrimidine-6-carboxylic acidHCID 2309195566.3%

Reaction Steps

5 N Sodium hydroxide solution (0.1 ml) was added to a solution of the thus obtained ethyl 2-hydroxymethylpyrazolo[1,5-a]pyrimidine-6-carboxylate (19 mg) in tetrahydrofuran (1 ml), and stirred for 17 hours at room temperature. After water was added, the reaction mixture was washed with ethyl acetate. The aqueous phase was acidified by 2 N hydrochloric acid, extracted with ethyl acetate and dried over sodium sulfate anhydrous. The resulting product was concentrated under reduced pressure, and the residue was dissolved in hot ethyl acetate and then filtered. The filtrate was concentrated under reduced pressure to give the title compound (11 mg, Y.:65%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345180B2
Source datasetuspto-grants-2008_03
ORD IDord-29a953d2324e4c91879369d745b8d1ef
Source noteuspto-grants-2008_03