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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991677Generated: November 1, 2026

2-Chloro-3-(piperazin-1-yl)pyrazine → HCID 22036310, compound

https://huagongshe.com/reaction/991677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-3-(piperazin-1-yl)pyrazineHCID 14086438—
ReactantHCID 22036348HCID 22036348—
ProductHCID 22036310HCID 2203631031%

Reaction Steps

The title compound was prepared according to the procedure of Example 90, Step 2, starting from the product obtained in Step 2 above and 2-chloro-3-( (1-piperazinyl)piperazine (from Example 90, Step 1). The crude product was purified by column chromatography (gradient: 1% NH4OH in EtOAc/MeOH (90:10) to 1% NH4OH in EtOAc/MeOH (80:20) in first purification step and gradient 0.5% NH4OH in CHCl3/MeOH (95:5) to 1% NH4OH in CHCl3/MeOH (90:10) in second purification). Yield 31%; mp 54.0-56.5° C.; MS m/z 381 (M+H)+. Anal. (C20H24N6O20.5 H2O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465467B1
Source datasetuspto-grants-2002_10
ORD IDord-8648838ff0124357a15ce9f1332ee047
Source noteuspto-grants-2002_10