HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436415Generated: October 31, 2026
Dimethylformamide → HCID 13259282, compound
https://huagongshe.com/reaction/436415
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dimethylformamide diethylacetal | HCID 70913 | — |
| Reactant | HCID 13259337 | HCID 13259337 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13259282 | HCID 13259282 | 18.9% |
Reaction Steps
To a mixture of 2.9 g of 1-(m-trifluoromethylphenyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine, 25 ml of dimethylformamide and 4.4 g of dimethylformamide diethylacetal was reacted at 145° - 150° C for 5 hours. After the reaction was complete, the solvent was distilled off from the mixture under reduced pressure. The residue thus obtained was diluted with water, extracted with ether and dehydrated. The ether solution was applied on a column of alumina and then eluted with ether. The eluate was concentrated by evaporation to leave a residue, which was then recrystallized from a mixture of ether and petroleum ether to give 0.6 g of 1-(m-trifluoromethylphenyl)-3-ethyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless prisms, melting at 155° - 157° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04009166 |
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| Source dataset | uspto-grants-1977_02 |
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| ORD ID | ord-18e15e9d30c8414899955d9c71998141 |
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| Source note | uspto-grants-1977_02 |
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