HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl isocyanate → 3-Ethyl-1-(3-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl isocyanate | HCID 8022 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium amide | HCID 24533 | — |
| Reactant | 2-(m-Nitroanilino)nicotinic acid ethyl ester | HCID 54318663 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-1-(3-nitrophenyl)pyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione | HCID 12764178 | 54.9% |
Reaction Steps
To a solution of 5.7 g of 2-(m-nitroanilino)nicotinic acid ethyl ester and 50 ml of dry tetrahydrofuran was added 1.1 g of sodium amide and the solution was stirred for one hour. To this was added dropwise under cooling 2.9 g of ethyl isocyanate and this mixture was reacted at 60°C for 10 hours. After the reaction was complete, the solvent was distilled off from the mixture, and to the residue obtained was added water to precipitate a crude product. This product was collected by filtration and recrystallized from methanol to give 3.4 g of 1-(m-nitrophenyl)-3-ethylpyrido[2,3-d]pyrimidine-2,4(1H,3H)-dione as colorless needles, melting at 210°-211°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03984415 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-270ee2839068435f86c80c9682a1a9b1 |
| Source note | uspto-grants-1976_10 |