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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775320Generated: October 31, 2026

Water → tert-Butyl 4-(5-methyl-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1775320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
Reactanttert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylateHCID 178452346—
SolventPyridineHCID 1049—
Producttert-Butyl 4-(5-methyl-1,2,4-oxadiazol-3-yl)piperazine-1-carboxylateHCID 8668604691.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of tert-butyl 4-(N-hydroxycarbamimidoyl)piperazine-1-carboxylate (771 mg, 3.16 mmol) in pyridine (8 mL) was added acetic anhydride (320 L, 3.42 mmol) and the reaction was heated to 80° C. for 3 h. The mixture was cooled to room temperature, poured into water and extracted with EtOAc. The organic layer was washed with water and brine, dried (Na2SO4) and concentrated under reduced pressure to yield 774 mg of a yellow solid. After purification by flash chromatography (silica, gradient of 0.5 to 3% methanol in dichloromethane) 509 mg of an off-white solid were obtained (1.897 mmol, 60%). MS (ESI) m/z=291.1 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-c4381c964faf4a398db4a678fee17190
Source noteuspto-grants-2016_02