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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44021Generated: October 23, 2026

Hydrochloric Acid → 6-Iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acid

https://huagongshe.com/en/reaction/44021

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 6-iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylateHCID 59233743—
SolventWaterHCID 962—
SolventLithium HydroxideHCID 3939—
SolventEthyl AcetateHCID 8857—
Product6-Iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acidHCID 5923377185%

Reaction Conditions

Temperature45 °C

Reaction Steps

Methyl-6-iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylate (250 mg, 0.661 mmol) was dissolve in aqueous LiOH(2N,1 mL), methanol (2 mL) and tetrahydrofuran (7 mL). This solution was stirred overnight at 45° C. After 24 hours, 2 mL 2M LiOH and 2 mL methanol were added. Heated at 55° C. overnight. The reaction was cooled on an ice water bath and aqueous hydrochloric acid (10 mL, 1N) was added dropwise until acidic by pH paper. Ethylacetate (200 mL) and water (40 mL) were added. The organic portion was extracted with brine (20 mL) and was dried over magnesium sulfate. The solvent was removed by rotory evaporation. The residue was place under vacuum overnight to give of a white solid (204 mg, 85%). 1H NMR (500 MHz, DMSO-D6) δ ppm 7.47 (m, 3H) 7.77 (m, 2H) 7.97 (d, J=9.46 Hz, 1H) 9.27 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08536338B2
Source datasetuspto-grants-2013_09
ORD IDord-ebd467546d364a949bbc9bec91c6b6a0
Source noteuspto-grants-2013_09