Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Methylmethanesulfonamide | HCID 97632 | — |
| Reactant | HCID 23226984 | HCID 23226984 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54502880 | HCID 54502880 | 10.1% |
Reaction Steps
N-Methylmethanesulfonamide (1.9 g) and then 1.2 g (17 mmol) of 5-(2,2-dimethylindan-1-yl)-4-methanesulfonylpyrimidine were added to a slurry of 0.40 g (17 mmol) of sodium hydride in 50 mL of dry N,N-dimethylformamide with stirring and the resulting mixture was heated at 80° C. for 1 hour. The mixture was then cooled and partitioned between ether and water. The organic phase was recovered, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure. The residue was purified by column chromatography on silica gel and 0.57 g of the title compound was obtained as a tan solid melting at 107°-109° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05780465 |
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| Source dataset | uspto-grants-1998_07 |
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| ORD ID | ord-c6511361fb90466786df1e9f15333616 |
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| Source note | uspto-grants-1998_07 |
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