HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521678Generated: October 30, 2026
Dimethylacetamide → 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-3H-pyrido[2,3-d]pyrimidin-4-one
https://huagongshe.com/reaction/521678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 2-(Ethylsulfanyl)benzaldehyde | HCID 13082726 | — |
| Reactant | Sodium Bisulfite | HCID 23665763 | — |
| Reactant | 2-Amino-5-(trifluoromethyl)pyridine-3-carboxamide | HCID 118035336 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-3H-pyrido[2,3-d]pyrimidin-4-one | HCID 136968752 | 57% |
Reaction Steps
A mixture of 1.0 g of 2-amino-5-trifluoromethylpyridine-3-carboxylic acid amide, 810 mg of 2-ethylsulfanylbenzaldehyde, 1.01 g of sodium bisulfite and 3 ml of DMA was stirred at 150° C. for 12 hours. Water was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, then dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 975 mg of 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-3H-pyrido[2,3-d]pyrimidin-4-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328121B1 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-712c4ce8f07e4292a8daa5add00bde48 |
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| Source note | uspto-grants-2016_05 |
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