HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177987Generated: November 1, 2026
2,6-Dichlorobenzoic acid → HCID 59559636, compound
https://huagongshe.com/reaction/1177987
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,6-Dichlorobenzoic acid | HCID 5758 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Biphenyl-4-carboxylicacid (2-oxo-2-piperazin-1-yl-ethyl)-amide | HCID 57855677 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59559636 | HCID 59559636 | 16.8% |
Reaction Steps
DIPEA (159.8 mg, 0.21 mL, 1.2 mmol) was added to a stirred solution of 2,6-dichloro-benzoic acid (59 mg, 0.3 mmol) in DMF (3 mL). HOBT (45.9 mg, 0.34 mmol) and EDCI (130.4 mg, 0.68 mmol) were then added at room temperature. After 2 minutes, Biphenyl-4-carboxylic acid (2-oxo-2-piperazin-1-yl-ethyl)-amide (120 mg, 0.37 mmol) was added and the resulting mixture was stirred at room temperature overnight. 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 get the residue. The obtained residue was purified by column chromatography (using silica gel of 60-120 mesh and 60% EtOAc in Hexane as eluent) to afford 25 mg (16.3% yield) of biphenyl-4-carboxylic acid {2-[4-(2,6-dichloro-benzoyl)-piperazin-1-yl]-2-oxo-ethyl}-amide. LCMS Purity: 86.98%. 1H NMR (CDCl3): δ 7.96-7.86 (d, 2H), 7.72-7.56 (dd, 4H), 7.5-7.34 (m, 6H), 7.32-7.2 (m, 2H), 4.4-4.24 (dd, 2H), 4.0-3.8 (bs, 2H), 3.8-3.6 (m, 3H), 3.6-3.5 (t, 1H), 3.4-3.24 (q, 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-227d9d90421c49d39e5e9c5b2d628029 |
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| Source note | uspto-grants-2010_11 |
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