Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethylene carbonate | HCID 7303 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(m-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 12760301 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12959657 | HCID 12959657 | 86.6% |
Reaction Steps
To a solution of 2.8 g of 1-(m-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4 (1H,3H)-dione and 30 ml of dimethylformamide was added 0.53 g of 55 % sodium hydride, and the solution was heated up to 150°C. To this was added 0.97 g of ethylene carbonate, and the mixture was reacted for one hour at 150°C. After the reaction was complete, the solvent was distilled off from the resulting mixture under reduced pressure. To the residue obtained was added water to precipitate a crude product. This product was recrystallized from methanol to yield 2.8 g of 1-(m-nitrophenyl)-3-(2-hydroxyethyl)pyrido[2,3-d] pyrimidine-2,4(1H,3H)-dione as pale yellow prisms, melting at 212°-213°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03984415 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-3174b789a5e1402ea53322581776f6a7 |
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| Source note | uspto-grants-1976_10 |
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