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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172381Generated: November 2, 2026

m-Chloroperbenzoic acid → HCID 71224273, compound

https://huagongshe.com/reaction/2172381

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051327B2
Source datasetuspto-grants-2015_06
ORD IDord-350235f0667541cea8d8c4ef4d45e5f5
Source noteuspto-grants-2015_06