HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 18510669, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 2529944 | HCID 2529944 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 18510669 | HCID 18510669 | 37% |
Reaction Steps
3-Pyridinecarboxaldehyde, oxime (0.013 mol) was added to a suspension of 1-chloro-2,5 pyrrolidinedione (0.0148 mol) in CHCl3 (80 ml) and pyridine (0.16 ml), stirred at RT. The mixture was stirred for 3 hours at 40° C., then cooled to 0° C. and 4-benzoyl-N-(2-propenyl)benzamide (0.011 mol) was added. Then, triethylamine (2.25 ml) was added dropwise and the resulting reaction mixture was stirred overnight at RT. The reaction mixture was washed with water, dried (Na2SO4), filtered and the solvent was evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 2.0 g (37%) of (±)4-benzoyl-N-[[4,5-dihydro-3-(3-pyridinyl)-5-isoxazolyl]methyl]benzamide. (compound 343).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07414048B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-931f936ffcf04e868653913a5c3d1523 |
| Source note | uspto-grants-2008_08 |