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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 388983Erstellt: 24. Oktober 2026

Diisopropylethylamine → 2-(2-trifluoromethylphenylamino)-benzooxazole-5-carboxylic acid (1H-indazol-6-yl)-amide

https://huagongshe.com/de/reaction/388983

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt2-(Trifluoromethyl)phenyl isothiocyanateHCID 737162—
Edukt3-amino-4-hydroxy-N-(1H-indazol-6-yl)-benzamideHCID 68444995—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2-trifluoromethylphenylamino)-benzooxazole-5-carboxylic acid (1H-indazol-6-yl)-amideHCID 59522579—

Reaktionsschritte

A solution of the aminophenol (0.5 mmol) from above in DMF (2 mL) was added with 1-isothiocyanato-2-trifluoromethylbenzene (0.6 mmol) and DIEA (1 mmol). The reaction mixture was subjected to microwave irradiation at 120° C. for 1 h. The reaction mixture was cooled to room temperature, diluted with water (20 mL). The solid formed was collected by filtration, washed with water, and dried in vacuo. The crude product was purified on a silica gel column chromatography using MeOH/DCM as eluent to provide 2-(2-trifluoromethylphenylamino)-benzooxazole-5-carboxylic acid (1H-indazol-6-yl)-amide, obtained as a yellow solid. MS: m/z 438 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377983B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-c7c76c0bbd7742dc8815e12b6a9e9f72
Quellennotizuspto-grants-2013_02