Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621541Generated: October 31, 2026

Ammonia → 3-cyclopropylmethyl 5-[2-(N-methyl-N-trimethylsilylmethylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate

https://huagongshe.com/reaction/621541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2-(N-methyl-N-trimethylsilylmethylamino)ethyl acetoacetateHCID 21243340—
ReactantCyclopropylmethyl 2-(3-nitrobenzylidene)acetoacetateHCID 53956239—
SolventEthanolHCID 702—
Product3-cyclopropylmethyl 5-[2-(N-methyl-N-trimethylsilylmethylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylateHCID 1410009625.7%

Reaction Steps

A mixture of 15.3 g (53 mmol) of 2-(N-methyl-N-trimethylsilylmethylamino)ethyl acetoacetate, 13.0 g (53 mmol) of cyclopropylmethyl 2-(3-nitrobenzylidene)acetoacetate, 4.4 ml of 28% aqueous ammonia and 50 ml of ethanol was stirred at the reflux temperature for 7 hours, and then the solvent was removed under reduced pressure. The residue was chromatographed on silica gel column to afford 3-cyclopropylmethyl 5-[2-(N-methyl-N-trimethylsilylmethylamino)ethyl] 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate (7.0 g, 25.7%) as yellow oil. Treatment of this oil with 1 equivalent of fumaric acid in ethanol gave the corresponding fumarate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824855
Source datasetuspto-grants-1989_04
ORD IDord-c949359ff57f46b29008d9dee23b3171
Source noteuspto-grants-1989_04