HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177960Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 178523544, compound
https://huagongshe.com/reaction/1177960
Participants
| Role | Name | HCID | Charge |
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| 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 | — |
| Reactant | HCID 178418479 | HCID 178418479 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178523544 | HCID 178523544 | 56.5% |
Reaction Steps
DIPEA (56 mg, 0.43 mmol) was added to a stirred solution of 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethanone TFA salt. (74 mg, 0.17 mmol) in DMF (1 mL). HOBT (23 mg, 0.17 mmol) and EDCI.HCl (33 mg, 0.17 mmol) were then added at room temperature. After 2 minutes, 6-hydroxy nicotinic 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 35 mg (56.5% yield) of 6-hydroxy-N-{2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-nicotinamide. LCMS Purity: 99.38%, HPLC Purity: 92.66%, 1H NMR (DMSO-d6): δ 12 (s, 1H), 8.0 (t, 1H), 7.9-7.8 (m, 2H), 7.8-7.7 (d, 1H), 7.7-7.6 (t, 1H), 7.6-7.5 (m, 1H), 6.4-6.3 (dd, 1H), 4.2-4.0 (m, 2H), 3.8-3.7 (m, 2H), 3.6 (m, 2H), 3.4 (m, 2H), 3.2-3.1 (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-86ac947cf9d5431a8b56c3526b345c24 |
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| Source note | uspto-grants-2010_11 |
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