HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Ondansetron
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methylimidazole | HCID 12749 | — |
| Reactant | 3-[(Dimethylamino)methyl]-1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one hydrochloride | HCID 21976925 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ondansetron | HCID 4595 | 83.1% |
Reaction Steps
3-[(Dimethylamino)methyl]-1,2,3,9-tetrahydro-9-methyl-4H-carbazol-4-one hydrochloride (12 kg, 41 mol) and 2-methylimidazole (20.2 kg, 246 mol, 6 eq.) were suspended in mixture of water (120 L) and DMF (30 L). The reaction mixture was heated to reflux (100–102° C.) and stirred for 5 hours at this temperature. The reaction mixture was cooled to 5–10° C. and stirred for half an hour. The precipitated crude ondansetron base was filtered and washed with cold water (2×110 L) and dried under vacuum at 60° C. to give ondansetron base (10 kg, 83% yield) in 97.3% HPLC purity. The major impurity was the exomethylene carbazolone which amounted to 2.6% of the crude ondansetron mixture.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07098345B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-4fddb17bac00436194745b17dd4dce0d |
| Source note | uspto-grants-2006_08 |