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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343269Generated: October 31, 2026

Nifedipine → N-Methylnifedipine

https://huagongshe.com/reaction/343269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNifedipineHCID 4485—
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
SolventTetrahydrofuranHCID 8028—
ProductN-MethylnifedipineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861235
Source datasetuspto-grants-1999_01
ORD IDord-2b89285e65764e26bd9d403ab29d233b
Source noteuspto-grants-1999_01