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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710633Generated: November 2, 2026

Chlorzoxazone → HCID 16059441, compound

https://huagongshe.com/reaction/1710633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorzoxazoneHCID 2733—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-1-(4-(4-chloro-3-methoxyphenyl)piperazin-1-yl)ethanoneHCID 21071126—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 16059441HCID 16059441—

Reaction Conditions

Temperature60 °C

Reaction Steps

In a 4 mL vial was added 2-chloro-1-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-ethanone (1) (200 mg, 0.66 mmol, 1.0 equiv), 5-chloro-3H-benzooxazol-2-one (105 mg, 0.69 mmol, 1.05 equiv), K2CO3 (365 mg, 2.64 mmol, 4.0 equiv) and 2.5 mL of NMP. A stir bar was placed in the vial and the vial was then capped. The mixture stirred at 60° C. overnight. The crude product was purified by reversed phase HPLC (acetonitrile —H2O with 0.1% TFA as the eluent) to yield 5-chloro-3-{2-[4-(4-chloro-3-methoxy-phenyl)-piperazin-1-yl]-2-oxo-ethyl}-3H-benzooxazol-2-one (16): HPLC retention time, 2.50 minutes (Agilent Zorbax SB-C18, 2.1×50 mm, 5μ, 35° C.) using 1 mL/min flow rate, a 2.5 minute gradient of 20% to 100% B with a 1.1 minute wash at 100% B (A=0.1% formic acid/5% acetonitrile/94.9% water, B=0.1% formic acid/5% water/94.9% acetonitrile); MS (ES) M+H expected, 436.3, found, 436.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790726B2
Source datasetuspto-grants-2010_09
ORD IDord-aa0f346ac90c4ebc844b0f737e51e441
Source noteuspto-grants-2010_09