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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1656897Generated: October 25, 2026

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

https://huagongshe.com/reaction/1656897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant2-Isopropyl-oxazole-4-carboxylic acid-cyclopropylamideHCID 15672429—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product4-Cyclopropylaminocarbonyl-2-isopropyloxazole-5-carboxylic acidHCID 1567243081%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256633
Source datasetuspto-grants-1993_10
ORD IDord-cb1f52e7da164dada609c04ae0e84343
Source noteuspto-grants-1993_10