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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44021Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
EduktTetrahydrofuranHCID 8028—
EduktMethyl 6-iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylateHCID 59233743—
LösungsmittelWaterHCID 962—
LösungsmittelLithium HydroxideHCID 3939—
LösungsmittelEthyl AcetateHCID 8857—
Produkt6-Iodo-2-phenylpyrazolo[1,5-a]pyridine-3-carboxylic acidHCID 5923377185%

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536338B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ebd467546d364a949bbc9bec91c6b6a0
Quellennotizuspto-grants-2013_09