HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177954Generated: November 3, 2026
4-Cyanobenzoic acid → HCID 25164323, compound
https://huagongshe.com/reaction/1177954
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Cyanobenzoic acid | HCID 12087 | — |
| 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 25164323 | HCID 25164323 | 50% |
Reaction Steps
DIPEA (53 mg, 0.41 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt (69 mg, 0.16 mmol) in DMF (1 mL). HOBT (22 mg, 0.16 mmol) and EDCI.HCl (31 mg, 0.16 mmol) were then added at room temperature. After 2 minutes, 4-cyanobenzoic acid (20 mg, 0.14 mmol) was added and the resulting mixture was stirred at room temperature for 4 hrs. Cold water (20 mL) 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 30 mg (50% yield) of 4-cyano-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide. LCMS Purity: 96.9%, 1H NMR (CDCl3): δ 7.9 (d, 2H), 7.8-7.7 (d, 3H), 7.6 (m, 2H), 7.4-7.3 (d, 2H), 4.2 (m, 2H), 4.4-4.2 (m, 2H), 4.0 (m, 2H), 3.8-3.4 (m, 5H), 3.4 (t, 1H), 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-f5e3023ad75b4e78b678f75be19a2ed3 |
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| Source note | uspto-grants-2010_11 |
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