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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991682Generated: October 30, 2026

Chlorosuccinimide → HCID 22036518, compound

https://huagongshe.com/reaction/991682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
Reactant2-Chloro-3-(piperazin-1-yl)pyrazineHCID 14086438—
SolventChloroformHCID 6212—
ProductHCID 22036518HCID 2203651845%

Reaction Steps

To a suspension of 2-chloro-3-(1-piperazinyl)pyrazine (11.7 g, 58.7 mmol; from Example 90, Step 1) in CHCl3 (50 mL) was N-chlorosuccinimid (14.4 g, 108 mmol) added and the mixture was heated at reflux for 30 minutes. The reaction mixture was cooled to ambient temperature and extracted twice with water. The combined aqueous phases were made alkaline (11M NaOH), saturated with NaCl, cooled, and extracted with EtOAc (×3). Concentration of the combined, dried (MgSO4), organic phases afforded 6.12 g (45%) of the title compound as a brown oil which crystallized upon standing: mp 89-97° C. Anal. (C8H10Cl2N4.1/3H2O) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465467B1
Source datasetuspto-grants-2002_10
ORD IDord-269becb54adf434d9ac80cbaeb04d63b
Source noteuspto-grants-2002_10