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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358849Generated: October 29, 2026

Potassium → HCID 178494030, compound

https://huagongshe.com/reaction/358849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassiumHCID 5462222—
Reactant2-Amino-2,3-dimethylbutanamideHCID 9793773—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 53970916HCID 53970916—
ReactantHCID 178437115HCID 178437115—
SolventTolueneHCID 1140—
ProductHCID 178494030HCID 178494030—

Reaction Steps

5 g of potassium tert.-butoxide are added in portions at a temperature of 80° C. to a solution of 5.7 g of 6-methoxymethyl-5-methylpyridine-2,3-dicarboxylic acid diethyl ester and 2.6 g of 2-amino-2,3-dimethylbutyramide in 200 ml of dry toluene while stirring. Once the addition of the potassium tert.-butoxide is complete, the resulting red solution is stirred for 2 hours at 80° C., the potassium salt of 2-(5-isopropyl-5-methyl-4-oxoimidazolin-2-yl)-5-ethylpyridine-3-carboxylic acid being deposited in the form of a thick crystalline slurry. The mixture is cooled to room temperature and filtered with suction, and the crystals are dried and then dissolved in 50 ml of saturated sodium chloride solution. The solution is adjusted to pH 4 with concentrated hydrochloric acid and then extracted three times with 100 ml of ethyl acetate each time. The organic phase is dried over magnesium sulphate, filtered off with suction and concentrated by evaporation. The residue crystallises from ether/hexane 1:2 yielding 2.8 g of the above acid, which has a melting point of 151°-153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04997947
Source datasetuspto-grants-1991_03
ORD IDord-74e1eea7522a424985bec55ffcbbcc6e
Source noteuspto-grants-1991_03