HuagongsheHuagongshe Chemistry Print Report · For research reference only
Deferiprone → 3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Deferiprone | HCID 2972 | — |
| Reactant | Octanoyl chloride | HCID 8124 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinone | HCID 19862588 | — |
Reaction Steps
With stirring, 0.56 ml of triethylamine is added at room temperature to a suspension of 0.556 g of 3-hydroxy-1,2-dimethyl-4(1H)-pyridinone in 40 ml of acetonitrile and 40 ml of methylene chloride, followed by the addition of 1.02 ml of caprylyl chloride. A solution forms within 3 minutes and after 30 minutes the reaction is complete, and the volatile constituents are removed by evaporation under reduced pressure. The residue is dried under a high vacuum and crystallised from a mixture of methylene chloride and ethyl acetate. The 3-(n-octanoyloxy)-1,2-dimethyl-4-(1H)-pyridinone so obtained begins to sinter at 140° C. and decomposes at 180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04908371 |
| Source dataset | uspto-grants-1990_03 |
| ORD ID | ord-0b42757bf86e4eb58e5a4fb473db2d72 |
| Source note | uspto-grants-1990_03 |