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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351477Generated: November 3, 2026

m-Chloroperbenzoic acid → HCID 178522349, compound

https://huagongshe.com/reaction/1351477

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 numberUS07217716B2
Source datasetuspto-grants-2007_05
ORD IDord-d0df0107f23345ad9f97035790fe10d5
Source noteuspto-grants-2007_05