HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177949Generated: October 29, 2026
3-Phenoxybenzoic acid → HCID 25164319, compound
https://huagongshe.com/reaction/1177949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Phenoxybenzoic acid | HCID 19539 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt | HCID 86634088 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25164319 | HCID 25164319 | 72.5% |
Reaction Steps
DIPEA (73 mg, 0.097 mL, 0.56 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (96 mg, 0.22 mmol) in DMF (1 mL). HOBT (30 mg, 0.22 mmol) and EDCI.HCl (43 mg, 0.22 mmol) were then added at room temperature. After 2 minutes, 3-phenoxybenzoic acid (40 mg, 0.19 mmol) was added and the resulting mixture was stirred at room temperature for 4 hrs. Cold water was then added and the product was extracted with EtOAc and the organic layer was washed with brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure to afford 70 mg (72.5% yield) of N-{2-Oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-3-phenoxy-benzamide. LCMS Purity: 89.64%. 1H NMR (DMSO-d6): δ 8.7-8.6 (t, 1H), 7.9-7.4 (m, 8H), 7.2 (m, 1H), 7.1-7.0 (d, 1H), 4.2-4.0 (m, 2H), 3.8-3.4 (m, 6H), 3.3-3.2 (m, 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-617525bebfa54bd28916a2e3dde15ea1 |
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| Source note | uspto-grants-2010_11 |
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