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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788753Generated: November 4, 2026

Potassium Carbonate → 1,6-Dihydro-2-methoxy-6-methyl-1-[3-[methyl(phenylmethyl)amino]propyl]-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methylethyl ester

https://huagongshe.com/reaction/1788753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-benzyl-3-chloro-N-methylpropan-1-amineHCID 22067—
Reactant18-Crown-6HCID 28557—
Reactant1,4-Dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methyethyl esterHCID 14627197—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product1,6-Dihydro-2-methoxy-6-methyl-1-[3-[methyl(phenylmethyl)amino]propyl]-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methylethyl esterHCID 5707707650.9%

Reaction Steps

A solution of 1,4-dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, 1-methyethyl ester (2.0 g, 6.0 mmol) in dimethylformamide (7.0 ml) was treated with finely ground potassium carbonate (1.7 g, 12.0 mmoles), N-benzyl-3-chloro-N-methylpropylamine (2.37 g, 12.0 mmol) and a catalytic amount of 18-crown-6. The reaction was heated at 70°-75° C. under argon overnight. The reaction was allowed to cool down to room temperature and was diluted with ether. It was filtered, and the filtrate was washed with water, brine and was dried over anhydrous magnesium sulfate. Evaporation of solvent provided a brown oil which was purified by flash chromatography (20% acetone in hexanes) to yield the title compound (1.51 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684655
Source datasetuspto-grants-1987_08
ORD IDord-580a557c2ed64af0a505c01de0c132cc
Source noteuspto-grants-1987_08