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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667667Erstellt: 26. Oktober 2026

Hexafluorophosphate → 2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1667667

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexafluorophosphateHCID 9886—
EduktAmmonium ChlorideHCID 25517—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acidHCID 86642799—
EduktHCID 178484285HCID 178484285—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-Azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amideHCID 8664280078,9%

Reaktionsschritte

To a solution of 1.76 g (5.60 mmole) of 2-azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid and 30 mL of dimethylformamide was added 2.75 g (7.01 mmole) of 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo[4,5-b]pyridinium, 3-oxide, hexafluorophosphate(1-) (1:1) and 3.0 mL (17.2 mmole) of ethyldiisopropylamine. The mixture was stirred for 18 minutes, then 0.4541 g (8.49 mmole) of ammonium chloride was added. The mixture was concentrated under reduced pressure and diluted with 350 mL of ethyl acetate and 75 mL of water. The ethyl acetate layer was washed with 50 mL of water, 50 mL of saturated aqueous sodium bicarbonate, 50 mL of brine, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with ethyl acetate-hexanes (gradient 10:90-100:0) to give 1.384 g of 2-azido-4-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid amide as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044213B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-56a479eb834a49269374a54bd7b5d9ad
Quellennotizuspto-grants-2011_10