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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1934802Generated: October 31, 2026

HCID 178516710, compound → 2-Piperazin-1-YL-quinoxaline

https://huagongshe.com/reaction/1934802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178516710HCID 178516710—
SolventPhosphorus oxychlorideHCID 24813—
Product2-Piperazin-1-YL-quinoxalineHCID 11820560—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Hydroxyquinoxaline (1.5 g) is heated in phosphorus oxychloride (10 mL) for 12 h. after which the reaction is concentrated and the residue partitioned between methylene chloride and 1 N NaOH. The resulting crude chloride is taken up in toluene (10 mL) and this solution is then added dropwise to a refluxing solution of piperazine (5 g) in toluene (40 mL). The resulting solution is refluxed for an additional 24 h, cooled to 0° C. for 0.5 h, filtered and concentrated. The filtrate is extracted with 10% acetic acid and the aqueous extracts washed with ether, basified and extracted with toluene. The toluene layer is washed with water, dried and concentrated. The concentrated material, which may alternatively be named quinoxalin-2-ylpiperazine, is placed under vacuum overnight (1.2 g, 77%, m.p. 74-76° C.). 1H NMR (CDCl3) 8.6 (s, 1H), 7.87 (dd, J=8, 1 Hz, 1H) , 7.68 (dd, J=8, 1 Hz, 1H), 7.57 (ddd, J=8, 7, 1 Hz, 1H), 7.39 (ddd, J=8, 7, 1 Hz, 1H) , 3.76 (t, J=5 Hz, 4H), 3.02 (t, J=5 Hz, 4H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06384224B2
Source datasetuspto-grants-2002_05
ORD IDord-a9e4610a2e444b0e8d6f04e536144447
Source noteuspto-grants-2002_05