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HRID 5456Erstellt: 23. Oktober 2026

1,1'-Carbonyldiimidazole → 5-[2-[2H-1,3-benzooxazine-2,4(3H)-dion-3-yl]ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/de/reaction/5456

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt5-[2-[2-(Hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridineHCID 23362977—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-[2-[2H-1,3-benzooxazine-2,4(3H)-dion-3-yl]ethylthio]imidazo[1,2-a]pyridineHCID 2336281877,8%

Reaktionsschritte

To a solution of 5-[2-[2-(hydroxy)benzoylamino]ethylthio]imidazo[1,2-a]pyridine (627 mg, 2.00 mmoles) in dry tetrahydrofuran (30 ml) was added 1,1'-carbonyldiimidazole (649 mg, 4.00 mmoles) and the mixture was stirred at room temperature for 15 hours. After the solvent was distilled off, chloroform was added to the residue, which was washed with water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 528 mg of the desired product (77.8%, colorless crystals).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244908
Quelldatensatzuspto-grants-1993_09
ORD IDord-7a110e2d9d2744ab950d8d0560459122
Quellennotizuspto-grants-1993_09