HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Difluoropyridine → HCID 57430079, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Difluoropyridine | HCID 73934 | — |
| Reactant | Tert-butyl 4-cyanopiperidine-1-carboxylate | HCID 1514443 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Product | HCID 57430079 | HCID 57430079 | — |
Reaction Steps
2,6-Difluoropyridine (2 g, 17 mmol) and tert-butyl 4-cyanopiperidine-1-carboxylate (2.4 g, 11 mmol) were reacted in the presence of potassium hexamethyldisilazide (14 mmol) using the method described in example 8-1 to afford the desired product: tert-butyl 4-cyano-4-(6-fluoropyridin-2-yl)piperidine-1-carboxylate: 1H NMR δ (ppm)(CDCl3): 7.86 (1 H, q, J=7.9 Hz), 7.54 (1 H, dd, J=2.3, 7.4 Hz), 6.93-6.91(1 H, m), 4.28 (21H, br s), 3.17 (2 H, br s), 2.25-2.17 (2 H, m), 2.02 (2 H, d, J=14.6 Hz), 1.48 (9H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825135B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-14f6769ce0334e66bbb797e26e79b014 |
| Source note | uspto-grants-2010_11 |