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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218884Generated: October 30, 2026

2-Fluoro-4-iodoaniline → 5-[(2-Fluoro-4-iodophenyl)amino]-2-phenylisonicotinic acid

https://huagongshe.com/reaction/218884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-4-iodoanilineHCID 185694—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Fluoro-2-phenylisonicotinic acidHCID 46314950—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product5-[(2-Fluoro-4-iodophenyl)amino]-2-phenylisonicotinic acidHCID 5764961456.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Lithium bis(trimethylsilyl)amide (2.8 ml, 1.0 M in THF, 2.76 mmol) was added to a suspension of 5-fluoro-2-phenylisonicotinic acid (500 mg, 2.30 mmol) in THF (10 ml) at −78° C. The dark colored suspension was stirred for 30 min. In another flask, 2-fluoro-4-iodoaniline (709.30 mg, 2.99 mmol, 1.30 eq) was dissolved in (15 ml) THF and cooled to −78° C. To this solution lithium bis(trimethylsilyl)amide (5 ml, 1.00 M, 5.06 mmol, 2.20 eq) was added and the mixture was stirred for 1 h. The reaction mixture became very viscous. To this, the homogeneous solution of acid-LiHMDS mixture was added via syringe. The mixture was warmed to room temperature and stirred overnight. Diluted with EtOAc (300 ml), washed with dilute HCl (20 ml), water (20 ml), and then dried and concentrated. Purified on Flashmaster using 100 g cartridge to obtain 565 mg of 5-[(2-fluoro-4-iodophenyl)amino]-2-phenylisonicotinic acid. LC/MS: [8.59 min; 435 (M+1)]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198457B2
Source datasetuspto-grants-2012_06
ORD IDord-38cdc947e29f4634807d18bde57e9f12
Source noteuspto-grants-2012_06