Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515633Generated: October 31, 2026

Trifluoroacetic acid → HCID 71761102, compound

https://huagongshe.com/reaction/515633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86701405HCID 86701405—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 71761102HCID 71761102—

Reaction Conditions

Temperature0 °C

Reaction Steps

TFA (0.20 mL) was added to a mixture of sodium (2S,5R)-2-(5-(4-(tert-butoxycarbonyl)piperazin-1-yl)-1,3,4-thiadiazol-2-yl)-7-oxo-1,6-diaza-bicyclo[3.2.1]octan-6-yl sulfate after lyophilization (33 mg, 0.064 mmol) in dry DCM (0.60 mL) at 0° C. The reaction mixture was stirred at 0° C. for 2-3 hrs and then diluted with ether (˜10 mL). The precipitate was collected via centrifugation, washed with ether (3×) and dried under high vacuum to afford (2S,5R)-7-oxo-2-(5-(piperazin-1-yl)-1,3,4-thiadiazol-2-yl)-1,6-diazabicyclo[3.2.1]octan-6-yl hydrogen sulfate (10 mg) as aTFA salt. ESI-MS (EI+, m/z): 391.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108966B2
Source datasetuspto-grants-2015_08
ORD IDord-1a7e1111c1ae41b9bde183070d874757
Source noteuspto-grants-2015_08