HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893913Generated: October 29, 2026
Malononitrile → 8-Ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile
https://huagongshe.com/reaction/1893913
Participants
| Role | Name | HCID | Charge |
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| Reactant | Malononitrile | HCID 8010 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehyde | HCID 57606953 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-Ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile | HCID 57606989 | — |
Reaction Steps
Potassium carbonate (0.539 g, 3.90 mmol) was added to a suspension of 4-(ethylamino)-6-methyl-2-(methylthio)pyrimidine-5-carbaldehyde (0.413 g, 1.95 mmol) from above, and malononitrile (0.194 g, 2.93 mmol) in absolute ethanol (15.0 mL) and heated to 70° C. After one h, the reaction was allowed to cool to room temperature and concentrated in vacuo. The residue was diluted with ethyl acetate (50 mL) and washed with saturated NaHCO3 (50 mL), and brine. The organic phase was separated and concentrated in vacuo. The residue was precipitated with ethyl acetate and hexanes to give 8-ethyl-7-imino-4-methyl-2-(methylthio)-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile as a brown solid that was used in the subsequent step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513266B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-cf54140ea40c4cd69277dbbd08ef281c |
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| Source note | uspto-grants-2013_08 |
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