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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Piperazin-1-yl-quinoline | HCID 1534386 | — |
| Reactant | Methanaminium, 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-one | HCID 66835944 | 15% |
| Product | (E)-4-chloro-1-[4-(4-quinolyl)piperazin-1-yl]but-2-en-1-one | HCID 66837142 | 33% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883791B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-98065993b97641dca27359660aa0cd3c |
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| Source note | uspto-grants-2014_11 |
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