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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567277Generated: October 30, 2026

Hydrochloric Acid → 9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazole

https://huagongshe.com/reaction/567277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
Reactant9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbomethoxy carbazoleHCID 22739786—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product9-[(3-Phenoxyphenyl)methyl]-4-hydroxy-5-carbamoyl carbazoleHCID 2274076543%

Reaction Steps

A solution of the 9-[(3-phenoxyphenyl)methyl]-4-hydroxy-5-carbomethoxy carbazole (100.0 mg, 0.24 mM) in 5 mL THF and 20 mL concentrated aqueous ammonium hydroxide was sonicated for 24 hours 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 twice 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 41.0 mg (43%) of the 9-[(3-phenoxyphenyl)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), 7.8 (dd, 1H, J=1 and 8 Hz), 7.5-6.7 (m, 13H), 6.6 (d, 1H, J=8 Hz), and 5.7 (s, 2H). MS (ES) m/e 407, 409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06177440B1
Source datasetuspto-grants-2001_01
ORD IDord-784676a4db564c01891728b10d04ccc8
Source noteuspto-grants-2001_01