HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (1-(3,5-Dichloropyridin-4-yl)piperidin-4-yl)(morpholino) methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Piperidinylcarbonyl)Morpholine | HCID 1520211 | — |
| Reactant | 3,4,5-Trichloropyridine | HCID 3786531 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | (1-(3,5-Dichloropyridin-4-yl)piperidin-4-yl)(morpholino) methanone | HCID 45274906 | 36.3% |
Reaction Steps
General procedure C was followed using morpholino(piperidin-4-yl)methanone (21 mg, 0.12 mmol), 3,4,5-trichloropyridine (23 mg, 0.12 mmol), triethylamine (32 μL, 0.23 mmol) and NMP (1 mL). The crude product was purified by flash column chromatography on silica gel (hexane/EtOAc, 1:1) to furnish the title compound as a white solid (15 mg, 35%), m.p. 172-174° C.; umax (CHCl3)/cm−1 3006, 2858, 1632, 1559, 1448, 1116, 1020; m/z (ESI) C15H20Cl2N3O2 requires 344.0927, found [M+H]+ 344.0929.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778925B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-ecc0671a1a98432891bc44ae4536a6e2 |
| Source note | uspto-grants-2014_07 |