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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427607Generated: October 28, 2026

Iodine → HCID 86701056, compound

https://huagongshe.com/reaction/1427607

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 numberUS08933232B2
Source datasetuspto-grants-2015_01
ORD IDord-c093073e12724789b19ac5d4bfdd422d
Source noteuspto-grants-2015_01