HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436412Generated: October 31, 2026
Dimethyl oxalate → HCID 13259319, compound
https://huagongshe.com/reaction/436412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl oxalate | HCID 11120 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Fluorophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one | HCID 13259318 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13259319 | HCID 13259319 | 63% |
Reaction Steps
To a solution of 2.4 g of 1-(p-fluorophenyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine and 15 ml of dimethylformamide was added 0.5 g of approximately 50% sodium hydride, and the mixture was allowed to stand until the evolution of hydrogen ceased. To this was further added 5.9 g of dimethyl oxalate and the resulting mixture was heated at 170° C in a sealed-tube for 12 hours. After the reaction was complete, the solvent was removed from the reaction mixture by distillation under reduced pressure. The residue thus obtained was diluted with water, extracted with ether and dehydrated. The ether solution was concentrated and left to give 1.6 g of 1-(p-fluorophenyl)-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless needles, melting at 212° - 213° 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-b6830649fd4d4b69817726be3ab72184 |
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| Source note | uspto-grants-1977_02 |
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