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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 280373Erstellt: 26. Oktober 2026

Phenol → (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl Ester

https://huagongshe.com/reaction/280373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenolHCID 996—
EduktTriethylamineHCID 8471—
EduktSodium BicarbonateHCID 516892—
EduktN,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chlorideHCID 21249497—
Edukt(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acidHCID 54200705—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
Produkt(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic Acid Phenyl EsterHCID 54508713—

Reaktionsschritte

A solution of 1.30 g (5 mmols) (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid, 1.27 g (5 mmols) N,N-bis(2-oxo-3-oxazolidinyl)phosphorodiamidic chloride, 0.49 g (5.2 mmols) phenol, and 1.10 g (10 mmols) triethylamine, in 10 ml dichloromethane was stirred at room temperature, under nitrogen atmosphere for 18 hours. Then, 10 ml of water (made slightly basic with sodium bicarbonate) were added. The precipitate was filtered of and the filtrate was dried over anhydrous magnesium sulfate, and evaporated to dryness under reduced pressure. The residual orange-yellow solid was recrystallized from anhydrous ethanol. Yield--0.62 g. Mp 194°-195° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04588812
Quelldatensatzuspto-grants-1986_05
ORD IDord-9bc3fb30f72f49fa81b82afc6e70df78
Quellennotizuspto-grants-1986_05