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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428530Generated: October 30, 2026

Vinyl chloroformate → HCID 18414146, compound

https://huagongshe.com/reaction/428530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl chloroformateHCID 78808—
Reactant2-[4-(Phenylmethyl)-1-piperazinyl]quinoxalineHCID 4551756—
ProductHCID 18414146HCID 18414146127.3%

Reaction Steps

To a room temperature solution of 1-benzyl-4-(quinoxalin-yl)-piperazine (1.0 g, 3.3 mmol) in anhydrous CH2C2 under nitrogen was added vinyl chloroformate (0.34 mL, 3.9 mmol) drop wise. The reaction mixture was heated at reflux 2 hours. The reaction was cooled, concentrated to dryness and concentrated HCl (25 mL) and 1,4-dioxane (25 mL) were added. The resulting solution was stirred at ambient temperature overnight. The solution was basified with 2.5 N NaOH (300 mL) and extracted into EtOAc (3×200 mL). The organic layers were combined, dried over Na2SO4, concentrated and chromatographed (10% MeOH/CH2Cl2/NH4OH) to give 450 mg (64%) of an orange solid: mp 106-108° C.: MS (+) ESI m/e 215 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313126B1
Source datasetuspto-grants-2001_11
ORD IDord-18456b6cb55345e48f1f69a3a556730a
Source noteuspto-grants-2001_11