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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333985Generated: October 26, 2026

(E)-4-methylhex-2-enoic Acid → (E)-4-Methyl-1-[4-[7-(trifluoromethyl)-4-quinolyl]piperazin-1-yl]hex-2-en-1-one

https://huagongshe.com/reaction/333985

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(E)-4-methylhex-2-enoic AcidHCID 5463168—
Reactant4-Piperazin-1-yl-7-(trifluoromethyl)quinolineHCID 11460205—
SolventDimethylformamideHCID 6228—
SolventDiisopropylethylamineHCID 81531—
SolventMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Product(E)-4-Methyl-1-[4-[7-(trifluoromethyl)-4-quinolyl]piperazin-1-yl]hex-2-en-1-oneHCID 86691602—

Reaction Steps

(E)-4-Methylhex-2-enoic acid (26 mg, 0.2 mmol) was dissolved in DMF (0.5 ml) together with diisopropylethylamine (35 μl), HATU was added (76 mg, 0.2 mmol) and the mixture was stirred at room temperature for 15 minutes. 4-piperazin-1-yl-7-(trifluoromethyl)quinoline (56 mg, 0.2 mmol) was dissolved in DMF (0.5 ml) together with diisopropylethylamine (35 μl), the two solutions were combined and stirred at room temperature overnight. The mixture was evaporated to dryness under reduced pressure and the residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 62.6 mg (0.16 mmol, 80%). MS (APCI) m/z=391.9 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-ffcff14e00e84e19a9757aa08db5402d
Source noteuspto-grants-2014_11