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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402944Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 71224273, compound

https://huagongshe.com/reaction/2402944

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
ReactantHCID 71224526HCID 71224526—
SolventDichloromethaneHCID 6344—
ProductHCID 71224273HCID 71224273—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a cold (0° C.) solution of Example 3A (200 mg, 0.661 mmol) in dichloromethane (2.2 mL) was added meta-chloroperoxybenzoic acid (179 mg, 0.728 mmol) in a single portion. After 1 hour, the reaction mixture was partitioned between 10% sodium thiosulfate solution and ethyl acetate. The layers were separated, and the organic layer was washed with saturated sodium bicarbonate solution, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was dissolved in N,N-dimethylformamide (3 mL). Hunig's base (231 μl, 1.323 mmol) and 4-(4-methylpiperazin-1-yl)aniline (127 mg, 0.661 mmol) were added to the solution, and the reaction was heated to 45° C. for 3 hours. The reaction mixture was cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was concentrated under reduced pressure. The crude residue was purified by MPLC (10 g SiO2), eluting with dichloromethane to 10% methanol in dichloromethane, to provide the title compound. MS ESI(+) m/z 446.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796289B2
Source datasetuspto-grants-2014_08
ORD IDord-1d17ba3c6926403ea8630151102915fa
Source noteuspto-grants-2014_08