HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Methoxide → 2-(4-Fluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 4-Fluorobenzamidine Hydrochloride | HCID 12456160 | — |
| Reactant | 1-(3-trifluoromethylbenzoyl)-1-methanesulfonyl-2-(N,N-dimethylamino)ethene | HCID 54164006 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Fluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine | HCID 14883670 | 81.1% |
Reaction Steps
6 g of 1-(3-trifluoromethylbenzoyl)-1-methanesulfonyl-2-(N,N-dimethylamino)ethene and 4 g of 4-fluorobenzamidine hydrochloride were dissolved in 30 ml of methanol at room temperature. After adding 1.2 of sodium methoxide thereto, the mixture was heated under reflux for 1 hour. The solvent was distilled away under reduced pressure. The residue was washed with water, and then dried to obtain 6 g of 2-(4-fluorophenyl)-4-(3-trifluoromethylphenyl)-5-methanesulfonylpyrimidine (Compound 112).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05349108 |
| Source dataset | uspto-grants-1994_09 |
| ORD ID | ord-6e8a5e924733478e9da018705575c020 |
| Source note | uspto-grants-1994_09 |