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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333956Generated: October 30, 2026

Triethylamine → (E)-1-[4-(2,6-Dimethoxy-4-pyridyl)piperazin-1-yl]-4,4,5,5,5-pentafluoro-pent-2-en-1-one

https://huagongshe.com/reaction/333956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Reactant1-(2,6-Dimethoxy-4-pyridyl)piperazineHCID 66835826—
Reactant(2E)-4,4,5,5,5-Pentafluoro-2-pentenoic acidHCID 86691160—
SolventDichloromethaneHCID 6344—
Product(E)-1-[4-(2,6-Dimethoxy-4-pyridyl)piperazin-1-yl]-4,4,5,5,5-pentafluoro-pent-2-en-1-oneHCID 8669159717.7%

Reaction Steps

1-(2,6-Dimethoxy-4-pyridyl)piperazine (30 mg, 0.13 mmol) was dissolved in anhydrous dichloromethane (2 ml) together with (E)-4,4,5,5,5-pentafluoropent-2-enoic acid (35 mg, 0.18 mmol), triethylamine (31 mg, 44 μl, 0.32 mmol), HBTU (74 mg, 0.15 mmol) and stirred at room temperature for two hours. 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 9 mg of a solid (0.023 mmol, 15%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-8dc5061ba248457db9fa847e4f5dbac1
Source noteuspto-grants-2014_11