HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062317Generated: October 25, 2026
Acetonitrile → 2-(methylsulfanyl)-6-(3,5-dimethoxyphenyl)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/reaction/1062317
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | 4-(Ethylamino)-2-(methylthio)pyrimidine-5-carbaldehyde | HCID 10750444 | — |
| Reactant | Ethyl 2-(3,5-dimethoxyphenyl)acetate | HCID 11831071 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(methylsulfanyl)-6-(3,5-dimethoxyphenyl)-8-ethyl-8H-pyrido[2,3-d]pyrimidin-7-one | HCID 11199113 | 84% |
Reaction Steps
4.8 kg of 4-ethylamino-2-methylsulfanyl-pyrimidine-5-carboxaldehyde and 5.5 kg of (3,5-dimethoxyphenyl)-acetic acid ethyl ester were dissolved in 10 L of DMSO at room temperature and stirred. 4.4 kg of 1,8-diazabicyclo[5.4.0]undec-7-ene was added to the reaction mixture. The mixture was heated at about 45-50° C. for at least 3 hours. The reaction was monitored by reverse-phase HPLC (YMC-AQ column, 60:40 CH3CN/0.02 M SDS, pH 2.2, 1.0 mL/min, 254 nm). When the reaction was completed, ethyl alcohol (3 L) was added to the reaction vessel, which was cooled to 5-15° C. The yellow product was precipitated and collected by filtration, washed with a mixture of isopropyl alcohol and water (3 L+3 L), and dried in a vacuum tray dryer at about 40-45° C. for at least 12 hours using a house vacuum (˜30 in Hg) to provide 7.3 kg (84% yield) of 2-(methylsulfanyl)-6-(3,5-dimethoxyphenyl)-8-ethyl-8H-pyrido[2,3-d]pyrimidine-7-one. Proton NMR is consistent with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06960662B2 |
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| Source dataset | uspto-grants-2005_11 |
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| ORD ID | ord-b5cc121d416c4113b6bc16736e7c5635 |
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| Source note | uspto-grants-2005_11 |
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