HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330894Generated: October 30, 2026
Trifluoroacetic acid → HCID 73386853, compound
https://huagongshe.com/reaction/330894
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 86693915 | HCID 86693915 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 73386853 | HCID 73386853 | — |
Reaction Steps
To a solution of N,N,N-tributylbutan-1-aminium ({[(2S,5R)-2-({[(3R)-1-(tert-butoxycarbonyl)pyrrolidin-3-yl]oxy}carbamoyl)-7-oxo-1,6-diazabicyclo[3.2.1]oct-6-yl]oxy}sulfonyl)oxidanide 6 (0.245 g, 0.35 mmol) in DCM (14 mL) was added trifluoroacetic acid (0.70 mL, 9.08 mmol) dropwise at 0° C. The reaction mixture was stirred for 1 h, then evaporated. Ether was added to the residue and the resulting white precipitate was collected by centrifugation. The solid was triturated with acetonitrile (2×) and the white solid was collected by centrifugation. The white solid was purified by HPLC on a prep-X Bridge-19×250 mm column and freeze-dried to give (2S,5R)-7-oxo-N-[(3R)-pyrrolidin-3-yloxy]-6-(sulfooxy)-1,6-diazabicyclo[3.2.1]octane-2-carboxamide Compound 1 (Table 1) (0.03 g, 25%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877743B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-962629b4f8c648bb9a53fddc04ed1f3f |
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| Source note | uspto-grants-2014_11 |
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