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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567263Generated: October 25, 2026

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

https://huagongshe.com/reaction/567263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
Reactant9-[(Phenyl)methyl]-4-hydroxy-5-carbomethoxy carbazoleHCID 22337716—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product9-[(Phenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 2233771826%

Reaction Steps

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) δ 10.5 (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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-5e605220246b4bbc8cb00cd7e0889220
Source noteuspto-grants-2001_01