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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333950Generated: October 30, 2026

Dichloromethane → (E)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one

https://huagongshe.com/reaction/333950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Piperazin-1-yl-quinolineHCID 1534386—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Product(Z)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-oneHCID 6683594415%
Product(E)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-oneHCID 6683714233%

Reaction Steps

The mixture of (E)- and (Z)-4-chlorobut-2-enoic acid (750 μl of the solution from step A, 0.19 mmol) together with HATU (72 mg, 0.19 mmol) and diisopropylethylamine (21.6 μl, 0.375 mmol) was stirred at room temperature for 15 minutes. 4-piperazin-1-ylquinoline (39.9 mg, 0.19 mmol) and diisopropylethylamine (10.8 μl) were added and stirring was continued for one hour. The mixture was diluted with dichloromethane, washed with 5% sodium bicarbonate solution, water, evaporated to dryness under reduced pressure and purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 20 mg (E)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (0.063 mmol, 33%) and 9 mg (Z)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one (0.029 mmol, 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-98065993b97641dca27359660aa0cd3c
Source noteuspto-grants-2014_11