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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460695Generated: October 30, 2026

Hydrochloric Acid → 6-(4-Benzylphenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid

https://huagongshe.com/reaction/460695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactant6-(4-Benzyl-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl esterHCID 69155787—
SolventTetrahydrofuranHCID 8028—
Product6-(4-Benzylphenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acidHCID 1595811821%

Reaction Steps

To a solution of 36 mg (0.082 mmol) of 6-(4-benzyl-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid ethyl ester in 3 mL of tetrahydrofuran was added 0.5 mL (0.5 mmol) of 1 M LiOH solution, and the resulting mixture was heated at reflux overnight. The reaction mixture was then acidified with 1 M HCl solution to pH=2, and extracted with ethyl acetate. The combined organic extracts were dried over sodium sulfate, and concentrated to give a residue which was purified via reverse-phase chromatography to afford (after lyophilization) 7 mg (21% yield) of 6-(4-benzyl-phenyl)-7-cyclohexyl-pyrazolo[1,5-a]pyrimidine-3-carboxylic acid as a solid (90% purity, entry 444) as indicated by 1H NMR; LC-MS—calcd for C26H25N3O2 [M++H]+: 412.19, found: 412.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196111B2
Source datasetuspto-grants-2007_03
ORD IDord-30d511ea27554c93b70fdf1bc02efbd0
Source noteuspto-grants-2007_03