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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942095Generated: November 2, 2026

Piperazin-2-one → HCID 50913157, compound

https://huagongshe.com/reaction/1942095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazin-2-oneHCID 231360—
ReactantPotassium FluorideHCID 522689—
ReactantHCID 58147535HCID 58147535—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 50913157HCID 50913157—

Reaction Conditions

Temperature170 °C

Reaction Steps

6-Chloro-3-[(S)-1-(4,6-difluoro-1-methyl-1H-indazol-5-yl)-ethyl]-imidazo[1,2-b]pyridazine (Intermediate Q, 50 mg, 0.144 mmol), KF, 42.6 mg, 0.719 mmol) and piperazin-2-one (44.5 mg, 0.431 mmol) were suspended in NMP (0.3 mL). The RM was stirred at 170° C. for 3 h. The mixture was diluted with EtOAc and washed with NaHCO3 10% (2×) and water (4×). The combined organic layers were dried over Na2SO4, filtered and concentrated. The residue was purified by flash chromatography and then crystallized in EtOAc/Pentane to afford the title compound as a light brown solid (tR 3.63 min (conditions 5), (tR 10.82 min (conditions 2), MH+=412.2, 1H-NMR in DMSO-d6: 8.07 (s, 1H); 8.03 (s, 1H); 7.79 (d, 1H); 7.52 (s, 1H); 7.36 (d, 1H); 7.02 (d, 1H); 4.85 (m, 1H); 3.95 (d, 1H); 3.95 (s, 3H); 3.73 (d, 1H); 3.54 (m, 2H); 3.17 (m, 2H); 1.79 (d, 3H)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389526B2
Source datasetuspto-grants-2013_03
ORD IDord-6b78668e629f45d683fc0038c848ac5e
Source noteuspto-grants-2013_03