HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665624Generated: October 31, 2026
1-Hydroxybenzotriazole → HCID 44231210, compound
https://huagongshe.com/reaction/1665624
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 4-(5-Methyl-1,3,4-oxadiazol-2-yl)aniline | HCID 19542244 | — |
| Reactant | 3-Oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acid | HCID 57875811 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44231210 | HCID 44231210 | 20% |
Reaction Steps
HOBt (72 mg, 0.53 mmol) and DMAP (81 mg, 0.66 mmol) were added to a stirred solution of 3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionic acid (150 mg, 0.44 mmol) in DMF (2 mL). The reaction mixture was cooled to 10° C. and EDCI.HCl (102 mg, 0.53 mmol) followed by 4-(5-methyl-[1,3,4]oxadiazol-2-yl)-phenylamine (77 mg, 0.44 mmol) were added. The reaction mixture was stirred at room temperature overnight then diluted with water and the product extracted with ethyl acetate. The organics were washed with brine solution, dried over Na2SO4 and concentrated. The residue was purified by column chromatography using basic alumina (80% ethyl acetate in hexane) to afford 40 mg (20%) of N-[4-(5-methyl-[1,3,4]oxadiazol-2-yl)-phenyl]-3-oxo-3-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propionamide. LCMS: 502.17 (M+1)+, 94.56%, 1H NMR: (DMSO-d6): δ 10.5 (d, 1H), 7.92 (m, 2H), 7.8 (m, 4H), 7.68 (t, 1H), 7.56 (m, 1H), 3.68 (m, 7H), 3.44 (m, 2H), 3.18 (m, 1H), 3.08 (m, 1H), 2.58 (s, 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-6d5f6d6b569647059fd178d8bc8c464d |
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| Source note | uspto-grants-2011_10 |
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