HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665593Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 44230805, compound
https://huagongshe.com/reaction/1665593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-biphenyl-4-yl-malonamic acid | HCID 55049154 | — |
| Reactant | HCID 66626075 | HCID 66626075 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44230805 | HCID 44230805 | 41% |
Reaction Steps
HOBt (25 mg, 0.185 mmol) and DIPEA (22 mg, 0.175 mmol) were added to a stirred solution of N-biphenyl-4-yl-malonamic acid (50 mg, 0.175 mmol) in DMF (3 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (50 mg, 0.26 mmol) was added followed by the addition of (2,5-dichloro-phenyl)-piperazin-1-yl-methanone hydrochloride (55 mg, 0.187 mmol). The reaction mixture was stirred at room temperature overnight. Water was then added and the resulting precipitate was filtered and purified by column chromatography using silica gel 60-120 mesh and 50% ethyl acetate in hexane as eluant to afford 35 mg (41%) of N-biphenyl-4-yl-3-[4-(2,5-dichloro-benzoyl)-piperazin-1-yl]-3-oxo-propionamide. LCMS: 497.11 M+1)+, 95.5%. 1H NMR: (CDCl3): δ 9.6 (d, 1H), 7.64 (m, 2H), 7.58 (m, 4H), 7.44 (m, 3H), 7.38 (d, 2H), 7.32 (m, 2H), 3.95 (m, 2H), 3.8 (m, 1H), 3.75 (m, 4H), 3.65 (m, 1H), 3.52 (d, 3H), 3.34 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08039463B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-d6d6076eb64a43b8924c0bd271098dfb |
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| Source note | uspto-grants-2011_10 |
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