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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422432Generated: November 2, 2026

Ammonium Chloride → 3-(4-Amino-2,6-dichloro-phenoxy)-quinoline-8-carboxylic acid methyl ester

https://huagongshe.com/reaction/2422432

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(2,6-Dichloro-4-nitro-phenoxy)-quinoline-8-carboxylic acid methyl esterHCID 57440942—
CatalystIronHCID 23925—
SolventEthanol tetrahydrofuran waterHCID 18504229—
Product3-(4-Amino-2,6-dichloro-phenoxy)-quinoline-8-carboxylic acid methyl esterHCID 57440939118.7%

Reaction Steps

To a solution of 3-(2,6-Dichloro-4-nitro-phenoxy)-quinoline-8-carboxylic acid methyl ester (98) (1.26 mmol) and NH4Cl (370 mg, 6.91 mmol) in EtOH/THF/H2O=8 mL/4 mL/2 mL was added iron powder (386 mg, 6.91 mmol). The reaction mixture was refluxed for 3.5 h. After cooling to room temperature and insoluble materials were filtered by Celite filtration. The filtrate was concentrated and sat NaHCO3 was added to the residue, which was extracted twice with AcOEt. Organic layer was washed by brine, dried over MgSO4, and concentrated. Crude residue was purified by column chromatography (hexane/AcOEt=2/1, 80 g of silica gel) to afford compound 99 (543 mg). 1H NMR (300 MHz, DMSO-d6) δ 3.91 (3H, s), 5.77 (2H, br s), 6.78 (2H, s), 7.50 (1H, d, J=3.0 Hz), 7.61 (1H, dd, J=8.1 Hz), 7.81 (1H, dd, J=1.4, 6.4 Hz), 8.08 (1H, dd, J=1.4 Hz, 6.4 Hz), 8.93 (1H, d, J=3.0 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960408B2
Source datasetuspto-grants-2011_06
ORD IDord-6846984fc80549d38233169ed1467459
Source noteuspto-grants-2011_06