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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515616Generated: October 31, 2026

Trifluoroacetic acid → HCID 86701387, compound

https://huagongshe.com/reaction/515616

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86701053HCID 86701053—
SolventDichloromethaneHCID 6344—
ProductHCID 86701387HCID 86701387172.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

CF3COOH (5 mL) was slowly added at 0° C. to a solution of tert-butyl 4-(5-((2S,5R)-6-(benzyl-oxy)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-2-yl)-1,3,4-oxadiazol-2-yl)piperazine-1 carboxylate (723 mg, 1.5 mmol) in DCM (20 mL). The mixture was stirred at 0° C. for 3 hrs, then, the solvent was concentrated to afford (2S,5R)-6-(benzyloxy)-2-(5-(piperazin-1-yl)-1,3,4-oxadiazol-2-yl)-1,6-diaza-bicyclo[3.2.1]octan-7-one (997 mg) as a brown oil, which was used directly in the next step. ESI-MS (EI+, m/z): 385.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108966B2
Source datasetuspto-grants-2015_08
ORD IDord-2f28c21be80144979b2258c65f56b91f
Source noteuspto-grants-2015_08