Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827114Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 178522349, compound

https://huagongshe.com/reaction/1827114

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantPhenylmethyl 4-[(4-pyridinylamino)carbonyl]-1-piperidinecarboxylateHCID 13937700—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 178522349HCID 178522349—

Reaction Steps

Benzyl 4-[(4-pyridinylamino)carbonyl]-1-piperidinecarboxylate (EXAMPLE 1, Step 1) (615 mg, 1.81 mmol) was dissolved in CH2Cl2 and treated with mCPBA (3.12 g, 18.10 mmol) and aged 18 h. The reaction was diluted with ethyl acetate and washed with sat. NaHCO3. The organics were separated, dried over Na2SO4, filtered and concentrated under reduced pressure. The resulting oil was purified by silica gel chromatography to afford benzyl 4-{[(1-oxido-4-pyridinyl)amino]carbonyl}-1-piperidinecarboxylate as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-c70d86ef9dac42f68b1bf36f49226c8f
Source noteuspto-grants-2006_05