Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 12168-64-8 | HCID 18008589 | — |
| Reactant | [(1-pyridin-3-yl-1H-[1,2,3]triazole-4-carbonyl)-amino]-acetic acid | HCID 66592012 | — |
| Reactant | 4-(2-Trifluoromethyl-phenoxy)-piperidine trifluoracetate | HCID 86634635 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44235737 | HCID 44235737 | 15.6% |
Reaction Steps
DIPEA (156.8 mg, 1.5 mmol) followed by HOBt (53 mg, 0.29 mmol) and EDCI (75 mg, 0.39 mmol) were added to a stirred solution of [(1-pyridin-3-yl-1H-[1,2,3]triazole-4-carbonyl)-amino]-acetic acid (prepared by the method used for the synthesis of Intermediate 64, starting from 3-aminopyridine, and subsequently, application of Step 3 of the General Scheme) (75 g, 0.3 mmol) in DMF (4 mL). After 2 minutes of stirring, 4-(2-trifluoromethyl-phenoxy)-piperidine trifluoroacetate (85 mg, 0.3 mmol) was added and the resulting mixture was stirred at room temperature overnight. Addition of cold water lead to the formation of a precipitate which was collected and purified by preparative HPLC to afford 24 mg (15.6% Yield) of 1-pyridin-3-yl-1H-[1,2,3]triazole-4-carboxylic acid {2-oxo-2-[4-(2-trifluoromethyl-phenoxy)-piperidin-1-yl]-ethyl}-amide. LC/MS [M+H]+: 475, 99.07%. 1H NMR (300 MHz, DMSO-d6): δ 9.45 (s, 1H), 9.2 (d, 1H), 8.75 (m, 1H), 8.5 (t, 1H), 8.4 (m, 1H), 7.7-7.6 (m, 3H), 7.4-7.35 (d, 1H), 7.1 (t, 1H), 5.0 (q, 1H), 4.25 (d, 2H), 3.7-3.5 (m, 4H), 2.0-1.8 (m, 2H), 1.8-1.5 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08129376B2 |
|---|
| Source dataset | uspto-grants-2012_03 |
|---|
| ORD ID | ord-a3f9de50751244ad8a409151de3a1464 |
|---|
| Source note | uspto-grants-2012_03 |
|---|