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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1677762Generated: November 1, 2026

2-Thiophenecarbonyl chloride → Tert-butyl 4-(5-(2-thienyl)-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1677762

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylateHCID 178452346—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-(5-(2-thienyl)-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylateHCID 5848796420%

Reaction Steps

To a cold (0° C.) solution of tert-butyl 4-[(hydroxyamino)(imino)methyl]piperazine-1-carboxylate (8 g, 32.7 mmol) in anhydrous DCM (150 mL) was added thiophene-2-carbonyl chloride (4.8 g, 32.7 mmol) followed by DIEA (7.2 mL, 39.2 mmol). The reaction mixture was stirred at RT for 12 hours and then filtered. The filtrate was evaporated and the residue was refluxed in pyridine (100 mL) for 3 hours. The solvent was removed under vacuum and the residue was dissolved in DCM. The organic layer was washed with a 10% aq. solution of sodium bicarbonate, water, brine and dried. The solvent was concentrated and the residue was purified by chromatography (Pet. Ether/EtOAc 7/3) to give 2.2 g (20%) of The title compound as a solid. TLC—Pet ether/EtOAc (9/1): Rf=0.75. HPLC purity>97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08008302B2
Source datasetuspto-grants-2011_08
ORD IDord-ac61994c826d424797f17470b7c77301
Source noteuspto-grants-2011_08