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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647388Generated: November 1, 2026

Hydrochloric Acid → HCID 15679358, compound

https://huagongshe.com/reaction/1647388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantL-Alanyl-L-prolineHCID 83525—
Reactant6-Chloronicotinoyl ChlorideHCID 2782165—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
SolventPotassium HydroxideHCID 14797—
ProductHCID 15679358HCID 1567935840%

Reaction Steps

L-Alanyl-L-proline (1.0 g, 5.4 mmol) is dissolved in a mixture of 10.8 ml of 0.5 N potassium hydroxide and 750 mg (5.4 mmol) of anhydrous potassium carbonate, and 10 ml of acetonitrile are added. After cooling in an ice bath, a concentrated acetonitrile solution of 1.2 g of 6-chloronicotinoyl chloride is added dropwise while stirring and keeping the pH of the mixture at 12 to 13 with 1N potassium hydroxide, as necessary. Stirring is continued for 2 additional hours at room temperature, then the solution is neutralized to pH 6 with aqueous hydrochloric acid, and the solvent is distilled off under reduced pressure. The residue thus obtained is suspended in 50 ml of absolute ethanol, the remaining potassium chloride is separated by centrifugation, and the solvent of the clear solution is distilled off under reduced pressure. The crude product is purified through silica gel column chromatography, using absolute ethanol as eluant, to isolate 700 mg of the desired product (yield: 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432159
Source datasetuspto-grants-1995_07
ORD IDord-d01c3df7a2514ed292083e666713e5fc
Source noteuspto-grants-1995_07