Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59438453 | HCID 59438453 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 72299201 | HCID 72299201 | 42% |
Reaction Steps
A solution of 1.15 g (4.595 mmol) rac-3-Hydroxy-1-methyl-5-nitro-5-phenyl-piperidin-2-one (example A.10, step 1) in 11.5 ml DMF was cooled to 0° C. 220 mg (5.514 mmol) NaH (60% in oil) was added. The temperature rose to 3° C. The mixture was stirred at 0° C. for 15 minutes. 430 ul (6.893 mmol) iodomethane was added and the mixture was stirred at 0° C. for 30 minutes. 6.5 ml water was added and the solvent was removed in vacuo. The residue was taken in ethyl acetate. The solution was washed twice with water. The washings were reextracted once with ethyl acetate. The combined extracts were dried over sodium sulfate, filtered and concentrated in vacuo. The crude oil was purified on silica gel (Eluent: Heptane/ethyl acetate 0 to 100%) to provide 500 mg (42%) of the title compound as a light brown solid. MS (m/e): 265.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067911B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-dd58900681834e69a45d718246dc4153 |
|---|
| Source note | uspto-grants-2015_06 |
|---|