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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218877Generated: October 27, 2026

2-Fluoro-4-iodoaniline → 2-Bromo-5-[(2-fluoro-4-iodophenyl)amino]isonicotinic acid

https://huagongshe.com/reaction/218877

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-iodoanilineHCID 185694—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Bromo-5-fluoroisonicotinic acidHCID 46739277—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product2-Bromo-5-[(2-fluoro-4-iodophenyl)amino]isonicotinic acidHCID 5764964959.3%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (11.9 ml, 1.00 M, 11.82 mmol) was added to a solution of 2-fluoro-4-iodoaniline (1.40 g, 5.91 mmol) at −78° C. The pale green colored solution was stirred for 1½ h at −78° C. Then, lithium 1,1,1,3,3,3-hexamethyldisilazan-2-ide (5.45 ml, 1.00 M, 5.45 mmol) was added followed by 2-bromo-5-fluoroisonicotinic acid (1.00 g, 4.55 mmol) in THF (5 ml). The dark colored homogeneous mixture was warmed to room temperature and stirred overnight. The crude was diluted with EtOAc (300 ml). Then, it washed with dilute HCl solution (20 ml), H2O (20 ml), dried and purified on Flashmaster II using a 100 g cartridge to obtain 1.18 g (59%) of 2-Bromo-5-(2-fluoro-4-iodo-phenylamino)-isonicotinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198457B2
Source datasetuspto-grants-2012_06
ORD IDord-4104fccf8a034e8e848bc3c48339439b
Source noteuspto-grants-2012_06