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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788694Generated: October 27, 2026

Carbamimidic acid, methyl ester, sulfate (1:1) → 1,4-Dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, ethyl ester

https://huagongshe.com/reaction/1788694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbamimidic acid, methyl ester, sulfate (1:1)HCID 169039—
ReactantEthyl 2-(3-nitrobenzylidene)-3-oxobutanoateHCID 367507—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1,4-Dihydro-2-methoxy-6-methyl-4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, ethyl esterHCID 1391258375.5%

Reaction Steps

A reaction mixture containing 2-[(3-nitrophenyl)methylene]-3-oxobutanoic acid, ethyl ester (2.62 g, 10.0 mmole), O-methylpseudourea hydrogen sulfate (1.72 g, 10.0 mmole), and sodium bicarbonate (2.52 g, 30.0 mmole) in dimethylformamide (7 ml) was heated at 65°-70° C. for 16 hours. The reaction mixture was allowed to cool to room temperature, diluted with ethyl acetate, and filtered. The filtrate was washed with water and brine, and then dried over anhydrous magnesium sulfate. Evaporation of the solvent gave a yellow oil which was purified by flash chromatography (5% ethyl acetate in dichloromethane). The resulting foam was crystallized from isopropyl ether/hexanes to provide 2.41 g of 1, 4-dihydro-2-methoxy-6-methyl -4-(3-nitrophenyl)-5-pyrimidinecarboxylic acid, ethyl ester as a colorless crystalline product; melting point 103.5°-105° C. Analysis Calc'd. for C15H17N3O5 :

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04684656
Source datasetuspto-grants-1987_08
ORD IDord-b73c5667a45b47e58a27aba3d593882d
Source noteuspto-grants-1987_08