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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1959398Generated: November 1, 2026

Piperazine → HCID 66744426, compound

https://huagongshe.com/reaction/1959398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 86662081HCID 86662081—
SolventDimethylformamideHCID 6228—
SolventWater ethylacetateHCID 22728543—
ProductHCID 66744426HCID 6674442667%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of tert-butyl N-[5-bromo-3-(5-methyl-1,2,4-oxadiazol-3-yl)pyrazin-2-yl]-N-tert-butoxycarbonyl-carbamate (200 mg, 0.4383 mmol) in DMF (1.562 mL) was treated with piperazine (377.5 mg, 4.383 mmol) and the reaction mixture heated at 100° C. for 30 minutes. The reaction was allowed to cool to RT and diluted with EtOAc/Water and the layers separated. The organic layer was washed with water (3×), dried (MgSO4), filtered and concentrated in vacuo. The material was used crude in the next step (150 mg, 67% Yield). 1H NMR (400.0 MHz, CDCl3) d 1.37 (18H, s), 2.73 (3H, s), 3.14 (4H, m) ppm; MS (ES+) 462.14

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410112B2
Source datasetuspto-grants-2013_04
ORD IDord-3e4bd46553e44a8fbf64e03c7254e71a
Source noteuspto-grants-2013_04