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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481699Generated: October 30, 2026

Nifedipine → N-Methylnifedipine

https://huagongshe.com/reaction/481699

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 introduced into a 100-mL three-neck flask and dissolved in 50 mL tetrahydrofuran under nitrogen. 1.66 g of a 60% dispersion of sodium hydride in oil was then added with stirring. After stirring for a short 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 thereafter washed several times with water and dried over sodium sulfate. The sodium sulfate was subsequently filtered off and the solvent was then pulled off from the filtrate on a rotary evaporator. The obtained solid was dissolved in 200 mL MIBK, and the addition of hexane to this solution then yielded 8.9 g N-methylnifedipine as yellow crystals. mp=184°-187° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789460
Source datasetuspto-grants-1998_08
ORD IDord-9e690fa295b54e4a9c2949377669dc5d
Source noteuspto-grants-1998_08