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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399373Generated: October 30, 2026

Nifedipine → N-Methylnifedipine

https://huagongshe.com/reaction/399373

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

Temperature38 °C

Reaction Steps

12 g of nifedipine was disclosed in 50 ml of tetrahydrofuran in a nitrogen atmosphere. 1.66 g of a sodium hydride/oil dispersion (60% NaH) was added under agitation. Following agitation for some time, 10 ml of methyl iodide was added, and the resulting mixture was agitated for 1 hour at 38° 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. The solid obtained was dissolved in 200 ml of MIBK, and hexane was added producing 8.9 g of N-methylnifedipine in the form of yellow crystals. This compound had a melting point of 184° to 187° C.; an infrared absorption spectrum of 1690 cm-1 ; C=O, 1524 cm-1 ; N--O), and a proton-NMR spectrum (solvent: CDCl3) of 2.5 (6 H, 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 numberUS05820944
Source datasetuspto-grants-1998_10
ORD IDord-df6e601094554948acb93bc45d40cf8c
Source noteuspto-grants-1998_10