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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2289899Generated: October 31, 2026

Hydrochloric Acid → HCID 178522885, compound

https://huagongshe.com/reaction/2289899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-ChlorobenzylamineHCID 66036—
ReactantTrimethylaluminumHCID 16682925—
ReactantEthyl 7-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 178469609—
SolventTolueneHCID 1140—
ProductHCID 178522885HCID 178522885—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 4-chlorobenzylamine (0.52 mL) in 5 mL of toluene is added 2.13 mL of a 2.0 M solution of trimethylaluminum in toluene. The solution is stirred for 5 min at 0° C. and then a suspension of 0.50 g of ethyl 7-fluoro-4-hydroxy-3-quinolinecarboxylate (J. Med. Chem., 20, 1001 (1977)) in 5 mL of toluene is added. The solution is stirred at 0° C. for an additional 10 min and then it is stirred 18 h at 90° C. The mixture is cooled to 25° C. and it is poured onto a mixture of a large excess of 3 M hydrochloric acid and ice. After stirring the mixture vigorously for 30 min it is filtered. The solid is dissolved in 50 mL of warm glacial acetic acid and distilled water is added to the resulting solution until it is cloudy. The mixture is then allowed to stand for several hours at 5° C. Filtration of this mixture gives the desired amide as 150 mg of a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06093732
Source datasetuspto-grants-2000_07
ORD IDord-ab7f71f4bd584214b06ab8ee7c62385e
Source noteuspto-grants-2000_07