HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nifedipine → N-Methylnifedipine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nifedipine | HCID 4485 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Methylnifedipine | HCID 14817573 | — |
Reaction Steps
12 g nifedipine was placed in a 100-mL three-neck flask and dissolved in 50 mL tetrahydrofuran under nitrogen. To this was added 1.66 g of an oil dispersion of sodium hydride (60% NaH) with stirring. After stirring for a brief period of time, 10 mL methyl iodide was added and the reaction was stirred for 1 hour at 38° C. 200 mL ethyl acetate was then added and the organic layer was washed several times with water and dried over sodium sulfate. The sodium sulfate was filtered off and the solvent was removed from the filtrate on a rotary evaporator. The resulting solid was dissolved in 200 mL MIBK. The addition of hexane gave 8.9 g N-methylnifedipine as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05861235 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-2b89285e65764e26bd9d403ab29d233b |
| Source note | uspto-grants-1999_01 |