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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39509Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/39509

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Fluoro-4-iodoanilineHCID 185694—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt2-Bromo-5-fluoroisonicotinic acidHCID 46739277—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-Bromo-5-[(2-fluoro-4-iodophenyl)amino]isonicotinic acidHCID 5764964959,3%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524911B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-e2bb8318f0b948d7804f0b05b647a69b
Quellennotizuspto-grants-2013_09