HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178011Generated: November 4, 2026
2-Fluorobenzoic acid → Biphenyl-4-carboxylicacid {2-[4-(2-fluoro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide
https://huagongshe.com/reaction/1178011
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Fluorobenzoic acid | HCID 9935 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | biphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide TFA salt | HCID 131728551 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Biphenyl-4-carboxylicacid {2-[4-(2-fluoro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide | HCID 25166105 | 42.2% |
Reaction Steps
DIPEA (77.35 mg, 0.598 mmol) was added to a stirred solution of biphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amide TFA salt (70 mg, 0.16 mmol) in DMF (2 mL). HOBT (19.8 mg, 0.15 mmol) and EDCI.HCl (63.74 mg, 0.33 mmol) were then added. After 2 minutes 2-fluorobenzoic acid (18.6 mg, 0.133 mmol) was added and the resulting mixture was stirred overnight. The reaction mixture was diluted with cold water and the product was precipitated and isolated by filtration to afford crude product, which was purified by column chromotography (using silica gel of 160-120 mesh and 50% EtOAc in hexane as eluent) to afford 25 mg (41.4% yield) of Biphenyl-4-carboxylicacid {2-[4-(2-fluoro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LC-MS purity: 94.8%, 1H NMR: (CDCl3) δ 7.9 (d, 2H), 7.6 (dd, 4H), 7.4 (m, 4H), 7.2 (s, 1H), 7.1 (t, 1H), 4.4 (dd, 2H), 3.8 (t, 2H), 3.6 (t, 4H), 3.4 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842696B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-030eaf54243b420cafc8317faadf9f1c |
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| Source note | uspto-grants-2010_11 |
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