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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341121Generated: October 30, 2026

Piperazine → HCID 178420014, compound

https://huagongshe.com/reaction/341121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 178478062HCID 178478062—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178420014HCID 17842001411%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 3-(6-chloro-2-pyridyl)-1H-pyrazolo[3,4-b]pyrazine (150 mg, 0.6476 mmol) and piperazine (167.4 mg, 1.943 mmol) in NMP (1.5 mL) was heated in microwave at 150° C. for a total of 1.5 h. Mixture cooled to ambient, diluted with EtOAc and washed with sat. NaHCO3 solution (1×), water (2×), brine (1×), dried (MgSO4), filtered and concentrated in vacuo. Crude product purified by ISCO companion (24 g SiO2, 0.5 to 10% MeOH (containing 10% ammonium hydroxide), pure fractions combined and concentrated in vacuo. Product re-dissolved in MeCN/H2O and freeze-dried to leave title compound as a yellow solid (20 mg, 11%). 1H NMR (DMSO-d6) δ2.82 (t, 4H), 3.56 (t, 4H), 6.85 (d, 1H), 7.69 (t, 1H), 7.77 (d, 1H), 8.65 (d, 1H) and 8.73 (d, 1H). ES+281.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895740B2
Source datasetuspto-grants-2014_11
ORD IDord-6f539ba13c6446bd9a3c86f48122570d
Source noteuspto-grants-2014_11