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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855611Generated: November 3, 2026

Iodine → HCID 86701056, compound

https://huagongshe.com/reaction/1855611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 86701042HCID 86701042—
SolventDichloromethaneHCID 6344—
ProductHCID 86701056HCID 8670105683.7%

Reaction Steps

To a 0° C. solution of PPh3 (2.2 g 8.4 mmol) in dry DCM (20 mL) was added I2 (2.1 g, 8.4 mmol). After I2 was dissolved, TEA (2.4 mL, 16.8 mmol) was added quickly at rt. The reaction mixture was stirred for 15 min. tert-Butyl (1R,3S)-3-(2-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carbonyl)hydrazinecarbonyl)cyclopentylcarbamate (2.1 g, 4.2 mmol) was added. The reaction mixture was stirred at rt for 1 h. The reaction mixture was concentrated and the residue was purified by silica gel column (gradient elution 0-50% EtOAc/petroleum ether) to afford the crude tert-butyl (1R,3S)-3-(5-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-oxadiazol-2-yl)cyclopentylcarbamate (˜1.7 g) as a white solid. ESI-MS (EI+, m/z): 484.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962844B2
Source datasetuspto-grants-2015_02
ORD IDord-3785282e35b14c9cb6fa9c7063650a23
Source noteuspto-grants-2015_02