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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5332Erstellt: 24. Oktober 2026

Carbon Dioxide → 4-Cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acid

https://huagongshe.com/de/reaction/5332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
Edukt2-Isopropyl-oxazole-4-carboxylic acid-cyclopropylamideHCID 15672429—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produkt4-Cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acidHCID 1567243081%

Reaktionsschritte

At -70° C. and under a nitrogen blanket, 0.12 mol of n-butyllithium (80.0 ml of a 1.5 molar solution in hexane) was dripped into a solution of 10.4 g (0.054 mol) of 2-isopropyloxazole-4-carboxylic acid-cyclopropylamide in 250 ml of tetrahydrofuran, and the mixture was stirred for 30 minutes at this temperature. The reaction mixture was then poured onto 500 g of solid CO2 and allowed to stand overnight. The residue remaining after evaporating down was taken up in 200 ml of water and 30 ml of 2N NaOH, the solution was extracted twice, each time with 100 ml of diethyl ether, the aqueous phase was acidified to a pH of 2 with concentrated hydrochloric acid and the solution extracted three times, each time with 200 ml of ethyl acetate. Drying over magnesium sulfate and removal of the solvent under reduced pressure gave 10.4 g (81%) of 4-cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acid as a white powder of m.p. 109°-112° C. (active ingredient no. 3.007).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05244867
Quelldatensatzuspto-grants-1993_09
ORD IDord-6db241b1de6942798489126e4163fdde
Quellennotizuspto-grants-1993_09