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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404220Generated: November 2, 2026

2-Fluoro-4-iodoaniline → 6-Chloro-3-[(2-fluoro-4-iodophenyl)amino]pyridazine-4-carboxylic acid

https://huagongshe.com/reaction/2404220

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-iodoanilineHCID 185694—
Reactant3,6-Dichloropyridazine-4-carboxylic acidHCID 433804—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product6-Chloro-3-[(2-fluoro-4-iodophenyl)amino]pyridazine-4-carboxylic acidHCID 24822027—

Reaction Steps

To solution of 2-fluoro-4-iodoaniline (9.21 g, 38.86 mmol) and 3,6-Dichloro-pyridazine-4-carboxylic acid (10.84 g, 64.77 mmol) in THF (80 mL) at −78° C., was added LiHMDS (5 g, 25.91 mmol). The mixture was allowed to warm to room temperature and stirred for 12 h. The mixture as diluted with ethyl acetate and washed with H2O and brine. The organic layer was dried with solid Na2SO4 and was concentrated. The resulting residue was purified by flash chromatography in silica (25% ethyl acetate-hexane) to give pure product. LC/MS [4.52 min; 394 (M+1)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802703B2
Source datasetuspto-grants-2014_08
ORD IDord-035fa69e0e2843979a92913b93097c37
Source noteuspto-grants-2014_08