HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Teriflunomide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-Bromo-3-oxo-N-(4-(trifluoromethyl)phenyl)butanamide | HCID 44628741 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | Teriflunomide | HCID 54684141 | 85.4% |
Reaction Steps
A mixture of 2-bromo-3-oxo-N-[4-(trifluoromethyl)phenyl]butanamide (10 g) [obtained from above step-b] and sodium cyanide (1.69 g) in DMSO (30 ml) was stirred at room temperature overnight. The reaction mixture was diluted with water (100 ml) and acidified with 50% HCl solution. Precipitated solid was filtered and washed with water. The solid was dried to give Teriflunomide (7.12 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08420856B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-55d865392aa344809251822d20f8c464 |
| Source note | uspto-grants-2013_04 |