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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 407106Erstellt: 25. Oktober 2026

2-Fluorobenzoyl chloride → N-[4-(5-chloro-2-methylbenzoxazol-6-yl)phenyl](2-fluorophenyl)carboxamide

https://huagongshe.com/reaction/407106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Fluorobenzoyl chlorideHCID 9808—
EduktDiisopropylethylamineHCID 81531—
EduktSodium bicarbonate methylene chlorideHCID 23716255—
Edukt4-(5-Chloro-2-methylbenzoxazol-6-yl)phenylamineHCID 67467295—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[4-(5-chloro-2-methylbenzoxazol-6-yl)phenyl](2-fluorophenyl)carboxamideHCID 5459667557,5%

Reaktionsschritte

To a solution of 4-(5-chloro-2-methylbenzoxazol-6-yl)phenylamine (56) (23 mg, 0.089 mmol) and 2 mg DMAP in 2 ml DCM was added 2-fluorobenzoyl chloride (21 μl, 0.18 mmol) followed by addition of DIEA (78 μl). The resulting brown solution was stirred at r.t. for 3 h. The reaction mixture was worked up with aq. NaHCO3/DCM. DCM phase was washed with brine, concentrated to dryness. The residue was dissolved in 2 ml THF/MeOH/H2O (5:4:1) and stirred with 1N NaOH (200 μl) at r.t. for 2 h before worked up with EA/aq. NaHCO3. Silica gel flash chromatography furnished 19.5 mg 57 as off-white solid. (yield: 57.5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08754219B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-9002de1b4d55484fb0725d693d7a0c47
Quellennotizuspto-grants-2014_06