Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775356Generated: October 31, 2026

Oxalyl chloride → Ethyl 5-methylamino-2-[4-[(E)-4,4,4-trifluorobut-2-enoyl]piperazin-1-yl]thiazole-4-carboxylate

https://huagongshe.com/reaction/1775356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4,4,4-Trifluorocrotonic acidHCID 5709614—
ReactantEthyl 5-(methylamino)-2-(piperazin-1-yl)thiazole-4-carboxylate hydrochlorideHCID 89826078—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-methylamino-2-[4-[(E)-4,4,4-trifluorobut-2-enoyl]piperazin-1-yl]thiazole-4-carboxylateHCID 7176528711.3%

Reaction Steps

(E)-4,4,4-Trifluorobut-2-enoic acid (25 mg, 0.18 mmol) was dissolved in dichloromethane (1 ml), oxalyl chloride (16 μl, 0.18 mol) and one drop of DMF were added and the resulting solution was stirred at room temperature for 10 minutes. This solution was added to a solution of ethyl 5-methylamino-2-piperazin-1-yl-thiazole-4-carboxylate hydrochloride (41 mg, 0.15 mmol) and DIPEA (79 μl, 0.45 mmol) in anhydrous DCM (2 ml) and the resulting mixture was stirred at room temperature overnight. The mixture was concentrated 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 7 mg of a solid (0.017 mmol, 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-072eddde2ba648c79edd065030207a0f
Source noteuspto-grants-2016_02