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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323632Generated: October 30, 2026

Triethylamine → HCID 178515070, compound

https://huagongshe.com/reaction/323632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromophenylhydrazine hydrochlorideHCID 12157—
ReactantHCID 178418477HCID 178418477—
SolventEthanolHCID 702—
ProductHCID 178515070HCID 17851507062.8%

Reaction Steps

To a stirred suspension of dimethyl-7-chloro-4-hydroxyquinoline-2,3-dicarboxylate (1.90 g, 6.40 mM) and 4-bromophenylhydrazine hydrochloride (10.0 g, 44.7 mM) in ethanol (35 mL) was added triethylamine (7.1 mL, 51.1 mM). The resulting brown solution was refluxed for 22 hours during which time a tan precipitate formed. This mixture was cooled to room temperature and filtered to give the 4-bromophenylhydrazine salt of the title compound as a white powder (1.69 g). This material was refluxed in glacial acetic acid (20 mL) for 3 hours and cooled to room temperature. The resulting tan suspension was filtered and the solids washed with glacial acetic acid and then ether to give the title compound (1.15 g, 43%) as a tan powder, mp 393-394° C.; MS(CI): 420 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06214826B1
Source datasetuspto-grants-2001_04
ORD IDord-c627624004954f88939d04c208eaa6a9
Source noteuspto-grants-2001_04