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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528679Generated: October 28, 2026

4-Quinolinecarboxylic acid → HCID 71655554, compound

https://huagongshe.com/reaction/528679

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Quinolinecarboxylic acidHCID 10243—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 89705144HCID 89705144—
SolventDimethylformamideHCID 6228—
ProductHCID 71655554HCID 71655554—

Reaction Steps

Commercially available quinoline-4-carboxylic acid (0.078 g, 0.449 mmol) was dissolved in 7 ml of DMF, N-ethyl-N-isopropylpropan-2-amine (0.242 ml, 1.347 mmol), HOBT (0.069 g, 0.449 mmol) and TBTU (0.144 g, 0.449 mmol) were added. After 15 min a solution of (S)-1-(2-aminoacetyl)pyrrolidine-2-carbonitrile 2,2,2-trifluoroacetate (0.120 g, 0.449 mmol) (prepared as described under A.1 of the experimental part) in DMF was added. The mixture was stirred overnight at room temperature. The volatiles were evaporated, the residue was dissolved in ethyl acetate and extracted with 1 N citric acid, saturated sodium bicarbonate and brine. The solution was dried over sodium sulfate, filtrated and evaporated. It was purified using column chromatography (1-5 hexane-ethyl acetate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346814B2
Source datasetuspto-grants-2016_05
ORD IDord-5d99de7a73214fa9b803bbbe9943db91
Source noteuspto-grants-2016_05