HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093696Generated: October 31, 2026
1-Hydroxybenzotriazole → HCID 57874518, compound
https://huagongshe.com/reaction/1093696
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-(6-phenyl-pyridin-3-yl)-malonamic acid | HCID 57874490 | — |
| Reactant | HCID 86634624 | HCID 86634624 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57874518 | HCID 57874518 | 50% |
Reaction Steps
To a stirred solution of N-(6-phenyl-pyridin-3-yl)-malonamic acid (0.07 g, 0.00024 mole) in DMF (1 mL) was added DIPEA (0.153 g, 0.00120 mole), HOBt (0.039 g, 0.00029 mole) and EDCI.HCl (0.055 g, 0.00029 mole). After 2 minutes (2-trifluoromethyl-phenoxy)-piperidin-4-yl-amine hydrochloride (0.080 g, 0.00029 mole) was added and the resulting mixture was stirred overnight. The reaction mixture was then diluted with cold water and the product was extracted with ethyl acetate. The organic layer was washed with brine solution, dried over sodium sulfate and concentrated under reduced pressure to afford 57.5 mg (50%) of 3-oxo-N-(6-phenyl-pyridin-3-yl)-3-[4-(2-trifluoromethyl-phenoxy)-piperidin-1-yl]-propionamide. LC-MS purity: 484.18 (M+1)+, 98.83%, 1H NMR (DMSO-d6): δ 10.5 (s, 1H), 8.8 (d, 1H), 8.2 (d, 1H), 8.1 (d, 2H), 8.0 (d, 1H), 7.7-7.6 (m, 2H), 7.5-7.3 (m, 4H), 7.1 (t, 1H), 4.9 (m, 1H), 3.7-3.5 (m, 6H), 2.0-1.6 (m, 4H).
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-27752f1ab35f4ffb904323257f5227b5 |
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| Source note | uspto-grants-2012_03 |
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