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HRID 51354Erstellt: 26. Oktober 2026

Hydrochloric Acid → 9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazole

https://huagongshe.com/reaction/51354

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAmmonium HydroxideHCID 14923—
Edukt9-[(Phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazoleHCID 22337716—
LösungsmittelMethanolHCID 887—
LösungsmittelEthyl AcetateHCID 8857—
Produkt9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 2233771826%

Reaktionsschritte

A solution of the 9-[(phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazole (200 mg, 0.6 mM) in 4 mL MeOH and 40 mL concentrated aqueous ammonium hydroxide was sonicated for 30 h at 40-50° C. The mixture was diluted with ethyl acetate and acidified to pH 1 with 5 N HCl. The aqueous layer was extracted three times with ethyl acetate. The combined organic extracts were washed with saturated brine, dried over magnesium sulfate, filtered, and concentrated. The residue was purified by column chromatography on silica gel (elution with gradient methylene chloride/ethyl acetate) to afford 50 mg (26%) of the 9-[(phenyl)methyl]-4-hydroxy-5-carbamoyl carbazole as a white solid. 1H NMR (DMSO-d6) δ10.5 (s, 1H), 8.8 (br s, 1H), 8.4 (br s, 1H), 7.85 (dd, 1H, J=1 and 8 Hz), 7.5-7.1 (m, 9H), 6.6 (d, 1H, J=8 Hz), and 5.8 (s, 2H). IR (KBr, cm−1) 3428, 3198, 3063, 1631, 1599, 1579, 1562, 1496, 1442, 1330, 1261, 1215, 775, and 697. MS (ES) m/e 315, 317.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713645B1
Quelldatensatzuspto-grants-2004_03
ORD IDord-60268cfd8da6451d99d15e8168b50feb
Quellennotizuspto-grants-2004_03