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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841443Generated: October 27, 2026

Potassium Carbonate → 7-(3,5-Dimethoxy-phenyl)-5-ethyl-3-methylsulfanyl-5H-pyrido[2,3-e]-1,2, 4-triazin-6-ylideneamine

https://huagongshe.com/reaction/1841443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-DimethoxyphenylacetonitrileHCID 139445—
Reactant5-Ethylamino-3-methylsulfanyl-1,2,4-triazine-6-carbaldehydeHCID 12098503—
SolventTetrahydrofuranHCID 8028—
Product7-(3,5-Dimethoxy-phenyl)-5-ethyl-3-methylsulfanyl-5H-pyrido[2,3-e]-1,2, 4-triazin-6-ylideneamineHCID 1209850460%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 5.0 g (25.2 mmol) of 5-ethylamino-3-methylsulfanyl-1,2,4-triazine-6-carbaldehyde in 125 mL of THF was added 6.7 g (37.8 mmol) of 3,5-dimethoxyphenylacetonitrile followed by 17.4 g (126.1 mmol) of potassium carbonate. The reaction mixture was warmed at 65° C. for 2 days, concentrated under vacuum, diluted with ethyl acetate, and washed three times with a saturated solution of sodium bicarbonate, once with water and brine. The organic phase was dried over magnesium sulfate, filtered, decolorized with charcoal, filtered through celite, and concentrated to give a dark orange oil. The crude oil was chromatographed through silica eluted with 2:2:6 to 2:3:5 dichloromethane/ethyl acetate/hexane to give 5.4 g (59%) of the title compound as a yellow amorphous solid. MS (APCI) (m+1)/z 358.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683183B2
Source datasetuspto-grants-2004_01
ORD IDord-1ff6d4ea9ad244b79484e60cc61fffa5
Source noteuspto-grants-2004_01