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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1430673Generated: October 31, 2026

Iodine → HCID 86701004, compound

https://huagongshe.com/reaction/1430673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 86701003HCID 86701003—
SolventDichloromethaneHCID 6344—
ProductHCID 86701004HCID 8670100487.4%

Reaction Steps

To a solution of PPh3 (2.6 g, 10.0 mmol) in dry DCM (60 mL) was added I2 (2.6 g, 10.0 mmol). After I2 was dissolved completely, TEA (3.5 mL, 25.0 mmol) was added quickly at rt. The mixture was stirred for 15 mins. Tert-butyl 4-(2-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octane-2-carbonyl)hydrazinyl)-4-oxobutylcarbamate (2.4 g, 5.0 mmol) was added. The mixture was stirred at rt for 1 hr. The solvent was concentrated. EtOAc (250 mL) was added, and the solution was filtrated to remove POPh3. The filtrate was concentrated. The resulting residue was purified by silica gel column chromatography (gradient elution 0˜40% EtOAc/petroleum ether) to afford tert-butyl 3-(5-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-oxadiazol-2-yl)propylcarbamate (2.0 g, 86%) as a white solid. ESI-MS (EI+, m/z): 458 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940897B2
Source datasetuspto-grants-2015_01
ORD IDord-5dacd6d7ae5d4e67a4fa667fac1b730a
Source noteuspto-grants-2015_01