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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Dimethoxyphenylacetonitrile | HCID 139445 | — |
| Reactant | 5-Ethylamino-3-methylsulfanyl-1,2,4-triazine-6-carbaldehyde | HCID 12098503 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-(3,5-Dimethoxy-phenyl)-5-ethyl-3-methylsulfanyl-5H-pyrido[2,3-e]-1,2, 4-triazin-6-ylideneamine | HCID 12098504 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06683183B2 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-1ff6d4ea9ad244b79484e60cc61fffa5 |
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| Source note | uspto-grants-2004_01 |
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