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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063994Generated: November 3, 2026

2,6-Dichloro-5-fluoronicotinic acid → 6-Chloro-5-fluoro-2-(2-fluoro-4-trimethylsilanyl-phenylamino)-nicotinic acid

https://huagongshe.com/reaction/2063994

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Dichloro-5-fluoronicotinic acidHCID 2733659—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Fluoro-4-(trimethylsilyl)anilineHCID 59596599—
SolventTetrahydrofuranHCID 8028—
Product6-Chloro-5-fluoro-2-(2-fluoro-4-trimethylsilanyl-phenylamino)-nicotinic acidHCID 5914013349%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cold (−78° C.) solution of 2-fluoro-4-trimethylsilanyl-phenylamine (19.2 g, 105 mmol) in anhydrous THF (50 mL) was added a solution of LHMDS (160 mL, 1 M in hexanes, 160 mmol) dropwise over 45 minutes under a nitrogen atmosphere. After 2 hours at −78° C., a solution of 2,6-dichloro-5-fluoro-nicotinic acid (10.5 g, 50 mmol) in anhydrous THF (30 mL) was added. The mixture was stirred at −78° C. for 1 hour then allowed to warm to ambient temperature. After 18 hours stirring at ambient temperature the reaction was quenched with water and adjusted to pH 2 by the addition of concentrated HCl. The solution was extracted with ethyl acetate and the organic layer was isolated, washed with water followed by brine, dried (Na2SO4), filtered and evaporated in vacuo. The resultant residue was triturated with methanol and filtered to afford the title compound as a yellow solid (8.7 g, 49%). LCMS (method B): RT=4.92 min, [M+H]+=357.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288408B2
Source datasetuspto-grants-2012_10
ORD IDord-06688221731b4785ab0e8f3a05ebf029
Source noteuspto-grants-2012_10