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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558224Generated: October 31, 2026

4-Bromo-2-fluoroaniline → 4-(4-Bromo-2-fluoro-phenylamino)-6-chloro-pyridazine-3-carboxylic acid

https://huagongshe.com/reaction/558224

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-2-fluoroanilineHCID 123050—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant4,6-Dichloro-3-pyridazinecarboxylic acidHCID 21919280—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Bromo-2-fluoro-phenylamino)-6-chloro-pyridazine-3-carboxylic acidHCID 59519495—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the stirred solution of 4-bromo-2-fluorophenylamine (3.15 g, 16.58 mmol) in THF (50 ml) under argon at −78° C. is added dropwise LiHMDS (24.9 ml, 24.9 mmol, 1.0 M in hexane). After stirring for one hour at −78° C., a solution of 4,6-dichloropyridazine-3-carboxylic acid (1.6 g, 8.29 mmol) in THF (10 ml) is added dropwise. The resulting mixture is allowed to warm to room temperature slowly and was stirred continuously for 18 hours. The reaction is quenched by addition of 5 ml of water, diluted with ethyl acetate, acidified with aqueous 1.0 M HCl to pH 1-2. The layers are separated and aqueous layer is extracted with ethyl acetate (30 ml×3). The combined organic layers are washed with brine (30 ml×3), dried over Na2SO4, and concentrated under reduced pressure. The residue is purified by flash column chromatography to give the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063049B2
Source datasetuspto-grants-2011_11
ORD IDord-22b6b66699f3481ba2455eadc5822753
Source noteuspto-grants-2011_11