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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775327Generated: November 1, 2026

Oxalyl chloride → (E)-4,4,4-Trifluoro-1-[4-(4-methylthiazol-5-yl)piperazin-1-yl]but-2-en-1-one

https://huagongshe.com/reaction/1775327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4,4-Trifluorocrotonic acidHCID 5709614—
Reactant4-Methyl-5-piperazin-1-yl-thiazole dihydrochlorideHCID 89825477—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product(E)-4,4,4-Trifluoro-1-[4-(4-methylthiazol-5-yl)piperazin-1-yl]but-2-en-1-oneHCID 7176525470%

Reaction Steps

(E)-4,4,4-Trifluorobut-2-enoic acid (33 mg, 0.23 mmol) was dissolved in dichloromethane (1 ml), oxalyl chloride (20 μl, 0.23 mol) and one drop of DMF were added and the resulting solution was stirred at room temperature for 15 minutes. This solution was added to a solution of 4-methyl-5-piperazin-1-yl-thiazole dihydrochloride (38 mg, 0.15 mmol) and N-ethyl-N,N-diisopropylamine (0.7 mmol, 120 μl) in dichloromethane (2 ml) and the resulting mixture was stirred at room temperature for three hours. The solvent was removed under reduced pressure and the resulting residue was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 32 mg of a solid (0.09 mmol, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-6951a41ae52848609354cc0b6eebdf1e
Source noteuspto-grants-2016_02