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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515605Generated: October 30, 2026

Pyridine → HCID 86701381, compound

https://huagongshe.com/reaction/515605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 86694021HCID 86694021—
SolventDichloromethaneHCID 6344—
ProductHCID 86701381HCID 8670138163.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

(CF3SO2)2O (0.50 mL) was slowly added to a solution of (2S,5R)—N′-acetyl-6-(benzyloxy)-7-oxo-1,6-diazabicyclo[3.2.1]octane-2-carbohydrazide (0.5 g) and pyridine (0.5 mL) in dry DCM (10 mL) at −10° C. The reaction mixture was stirred at 0° C. for 1 h and then quenched carefully with sat. NaHCO3. The organic layer was separated and the aqueous layer was exacted with EtOAc (3×). The combined organic layer was dried over Na2SO4, concentrated and purified by silica gel column chromatography (gradient elution 10:1 to 1:1 petroleum ether/EtOAc) to afford (2S,5R)-6-(benzyloxy)-2-(5-methyl-1,3,4-oxadiazol-2-yl)-1,6-diaza-bicyclo[3.2.1]octan-7-one (0.3 g, 63%) as a slight yellow solid. ESI-MS (EI+, m/z): 315.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108966B2
Source datasetuspto-grants-2015_08
ORD IDord-3ff0909da9364f549997d0552cd11713
Source noteuspto-grants-2015_08