HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361129Generated: October 31, 2026
Tetrahydrofuran → 5'-((1R,2R)-1-Benzyl-2-ethoxycarbonyl-2-hydroxy-ethylcarbamoyl)-2'-fluoro-biphenyl-2-carboxylic Acid
https://huagongshe.com/reaction/2361129
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Reactant | 5'-((1R,2R)-1-Benzyl-2-ethoxycarbonyl-2-hydroxy-ethylcarbamoyl)-2'-fluoro-biphenyl-2-carboxylic acid t-butyl ester | HCID 71073611 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5'-((1R,2R)-1-Benzyl-2-ethoxycarbonyl-2-hydroxy-ethylcarbamoyl)-2'-fluoro-biphenyl-2-carboxylic Acid | HCID 71073827 | 99% |
Reaction Steps
5′-((1R,2R)-1-benzyl-2-ethoxycarbonyl-2-hydroxy-ethylcarbamoyl)-2′-fluoro-biphenyl-2-carboxylic acid t-butyl ester (100 mg, 192 μmol, 1.0 eq.) was combined with 1:1 TFA/DCM (1 mL each) and stirred for 1 hour. The solvent was evaporated and THF (3 mL) and 1 M aqueous NaOH (577 μL, 3.0 eq.) were added. The mixture was stirred for 2 hours and EtOAc was added. The aqueous was extracted and the organic was washed with NaOH (0.2 mL), stirred, and the aqueous was extracted. The aqueous were acidified to pH ˜5 with concentrated HCl to yield a gummy solid. The aqueous was removed and the gummy solid was dissolved in AcOH and purified by preparative HPLC to yield the title compound (11.6 mg, 99% purity). MS m/z [M+H]+ calc'd for C26H24FNO6, 466.16. found 466.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08686184B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-91d055e593e348c7bad0b52aef8406c3 |
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| Source note | uspto-grants-2014_04 |
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