HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436413Generated: October 28, 2026
Dimethylformamide → HCID 13259295, compound
https://huagongshe.com/reaction/436413
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(3-Chlorophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one | HCID 13259294 | — |
| Reactant | HCID 21452456 | HCID 21452456 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13259295 | HCID 13259295 | — |
Reaction Steps
To a solution of 2.6 g of 1-(m-chlorophenyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine and 20 ml of dimethylformamide was added 0.6 g of sodium hydride and the mixture was stirred for 15 minutes. To this was further added 3.4 g of fluoromethylsulfate, and stirring was continued for 1.5 hours at room temperature. After the reaction was finished, the solvent was distilled off from the resulting 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 ether was evaporated from the eluate, and the residue was recrystallized from a mixture of ether and petroleum ether to give 2.1 g of 1-(m-chlorophenyl)-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless prisms, melting at 139° - 140° 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-be2a340c10dc4a89bcfe1d115e638aab |
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| Source note | uspto-grants-1977_02 |
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