HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093613Generated: October 29, 2026
1-Hydroxybenzotriazole → HCID 178440813, compound
https://huagongshe.com/reaction/1093613
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 | (2-Tert-butyl-phenyl)-piperidin-4-yl-amine dihydrochloride | HCID 66591489 | — |
| Reactant | HCID 178525878 | HCID 178525878 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178440813 | HCID 178440813 | 49% |
Reaction Steps
To a stirred solution of [(5-phenyl-1H-pyrazole-3-carbonyl)-amino]-acetic acid (0.088 g, 0.00036 mol) in DMF (2 mL) was added DIPEA (0.211 g, 0.0016 mol), HOBt (0.048 g, 0.00036 mol) and EDCI.HCl (0.125 g, 0.000655 mol) at ambient temperature. After 2 minutes (2-tert-butyl-phenyl)-piperidin-4-yl-amine dihydrochloride (0.1 g, 0.00033 mol) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water. The resulting precipitate was isolated by filtration and dried to afford 0.07 g (49%) of 5-phenyl-1H-pyrazole-3-carboxylic acid {2-[4-(2-tert-butyl-phenylamino)-piperidin-1-yl]-2-oxo-ethyl}-amide. LCMS: 460.26 (M+1)+, 89.75%, 1H NMR (DMSO-d6): δ 13.8 (s, 1H), 8.1 (s, 1H), 7.8 (d, 2H), 7.6-7.4 (m, 3H), 7.2-7.0 (m, 3H), 6.8 (d, 1H), 6.6 (t, 1H), 4.3 (d, 1H), 4.2 (d, 2H), 3.9 (m, 2H), 3.7 (s, 1H), 3.2 (t, 1H), 2.8 (t, 1H), 2.0 (t, 3H), 1.4 (s, 9H), 1.0 (bs, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129376B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-44984733f5134152be765ce82427b739 |
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| Source note | uspto-grants-2012_03 |
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