HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 25261140, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 25260976 | HCID 25260976 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25261140 | HCID 25261140 | — |
Reaction Steps
To a solution of 4-tert-butyl-2-(2-chloro-4-fluorophenoxy)-N-(3-(methylsulfonyl)phenyl)benzamide (14 mg, 30 μmol) in 0.30 mL DMF was added NaH (60% suspension in mineral oil, 3 mg, 80 μmol). After 5 min, iodomethane (5 μL, 80 μmol) was added to the reaction, and it was stirred for 16 h at room temperature. The reaction was worked up by adding sat. NaHCO3(aq) and extracting with CH2Cl2. The organic layer was filtered through a pad of Na2SO4 and evaporated. The product, 4-tert-butyl-2-(2-chloro-4-fluorophenoxy)-N-methyl-N-(3-(methylsulfonyl)phenyl)benzamide, was purified using reverse phase HPLC (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)). LC/MS: m/z 490.2 (M+H)+ at 2.03 min (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08779197B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-369dfb2c1dad49c4bcc83c0aea5d40f6 |
| Source note | uspto-grants-2014_07 |