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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1870079Generated: October 31, 2026

Nifedipine → N-Methylnifedipine

https://huagongshe.com/reaction/1870079

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNifedipineHCID 4485—
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
SolventMethyl Isobutyl KetoneHCID 7909—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductN-MethylnifedipineHCID 14817573—

Reaction Conditions

Temperature88 °C

Reaction Steps

12 g of nifedipine was dissolved in 50 ml of tetrahydrofuran under a nitrogen atmosphere. 1.66 g of a sodium hydride/oil dispersion (60% NaH) was added. Following agitation for some time, 10 ml of methyl iodide was added, and the resulting mixture was agitated for 1 hour at 88° C. 200 ml of ethyl acetate was then added. The resulting organic layer was washed several times with water, and was then dehydrated with sodium sulfate. The sodium sulfate was filtered out, and the solvent was removed from the filtrate by means of a rotary evaporator. The solid obtained was dissolved in 200 ml of MIBK, and hexane was added to this, producing 8.9 g of N-methylnifedipine in the form of yellow crystals. This compound had a melting point of 184 to 187° C., infrared absorption spectrum of 1690 cm-1 : C=O, 1524 cm-1 : N--O, and proton-NMR spectrum (solvent: CDCl3): 2.5 (6H, methyl), 3.3 (3H, N-methyl), 3.6 (6H, O-methyl), 5.7 (1H, C--H), 7.2-7.6 (4H, C--H in aromatic nucleus).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06096483
Source datasetuspto-grants-2000_08
ORD IDord-7bbca05432fb4e42b1498c04a20d0351
Source noteuspto-grants-2000_08