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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515609Generated: October 30, 2026

Trifluoroacetic acid → HCID 86700689, compound

https://huagongshe.com/reaction/515609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86701384HCID 86701384—
SolventDichloromethaneHCID 6344—
ProductHCID 86700689HCID 86700689171.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

CF3COOH (5 mL) was slowly added to a solution of tert-butyl 4-(5-((2S,5R)-6-(benzyloxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-oxadiazol-2-yl)piperidine-1-carboxylate (719 mg, 1.5 mmol) in DCM (20 mL) at 0° C. The mixture was stirred at 0° C. for 3 hrs then, the solvent was concentrated in vacuum to afford (2S,5R)-6-(benzyloxy)-2-(5-(piperidin-4-yl)-1,3,4-oxadiazol-2-yl)-1,6-diaza-bicyclo[3.2.1]octan-7-one (988 mg) as a brown oil, which was used directly in the next step. ESI-MS (EI+, m/z): 384.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108966B2
Source datasetuspto-grants-2015_08
ORD IDord-94392335f90449009fb9e602972aebec
Source noteuspto-grants-2015_08