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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1396944Generated: November 1, 2026

m-Chloroperbenzoic acid → HCID 178444620, compound

https://huagongshe.com/reaction/1396944

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactantphenylmethyl (3S)-3-{[(5-fluoro-2-pyridinyl)amino]carbonyl}-2-[(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl) heptanoyl]-1-pyrazolidinecarboxylateHCID 86706376—
SolventDichloromethaneHCID 6344—
ProductHCID 178444620HCID 17844462077.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of phenylmethyl (3S)-3-{[(5-fluoro-2-pyridinyl)amino]carbonyl}-2-[(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)heptanoyl]-1-pyrazolidinecarboxylate (130 mg, 0.210 mmol) in dichloromethane (DCM) (4 mL) under nitrogen at 0° C. was added 3-chlorobenzenecarboperoxoic acid (141 mg, 0.629 mmol) in one portion. The reaction mixture was stirred at 0° C. for 10 min, then warmed up to room temperature and stirred overnight. The reaction was quenched by addition of sat. aq. NaHCO3 and extracted with DCM twice. The combined organic extracts were dried over Na2SO4, filtered and concentrated to afford the crude product as a white semi-solid. The crude product was purified by RP-HPLC to provide phenylmethyl (3S)-3-{[(5-fluoro-1-oxido-2-pyridinyl)amino]carbonyl}-2-[(2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)heptanoyl]-1-pyrazolidinecarboxylate (103 mg, 77%). LCMS: (M+H)+: 636.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901119B2
Source datasetuspto-grants-2014_12
ORD IDord-02a96f1e220347d798b97c82db4e5f0b
Source noteuspto-grants-2014_12