HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539044Generated: November 3, 2026
Trifluoroacetic acid → HCID 67034433, compound
https://huagongshe.com/reaction/539044
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 67035301 | HCID 67035301 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67034433 | HCID 67034433 | 82.5% |
Reaction Steps
To a stirred solution of (S)-tert-butyl 2-(3-(4-(5-(4-isopropyl-2-oxooxazolidin-3-yl)pyrazolo[1,5-a]pyrimidin-3-yl)phenyl)-1H-1,2,4-triazol-1-yl)acetate (66 mg, 0.13 mmol) in DCM (1 mL) was added dropwise TFA (1 mL) at 0° C. under N2. The reaction mixture was stirred at ambient temperature overnight. The solvents were evaporated in vacuo. The residue was dissolved in saturated aqueous NaHCO3 solution and washed with Ether. The aqueous layer was acidified by slow addition of 1N HCl. The mixture was extracted with EtOAc. The combined organic layers were washed with brine, dried and concentrated to give (S)-2-(3-(4-(5-(4-isopropyl-2-oxooxazolidin-3-yl)pyrazolo[1,5-a]pyrimidin-3-yl)phenyl)-1H-1,2,4-triazol-1-yl)acetic acid (48 mg, 82%). LCMS (APCI+) m/z 448.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865726B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-ff74cb8d92c64d12b511ca5f4d6c5b24 |
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| Source note | uspto-grants-2014_10 |
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