HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 53308232, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | HCID 67322178 | HCID 67322178 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53308232 | HCID 53308232 | 47% |
Reaction Steps
A mixture of 0.011 g (0.027 mmol) of {4-[5-chloro-3-(3-chloro-benzoylamino)-pyridin-2-yl]-piperazin-1-yl}-acetic acid in N,N-dimethylformamide (1 mL), 0.011 g (0.13 mmol) of piperdine, 0.011 g (0.10 mmol) of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate, and 0.011 mL (0.081 mmol) of triethylamine is stirred at room temperature for 4 hours. The mixture is concentrated under reduced pressure and the residue is diluted with water causing a solid to precipitate from solution. The material is collected by filtration, washed with water and dried on the filter pad to provide 0.0060 g (47%) of the title compound (282) as a colorless solid. [M+H]+=476.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952004B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-3d6fea9291904e7b8c65bd1a1863c75d |
| Source note | uspto-grants-2015_02 |