HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-(3-Iodophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 21452453 | HCID 21452453 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-(3-Iodophenyl)-3,4-dihydropyrido[2,3-d]pyrimidin-2(1H)-one | HCID 13259332 | — |
Reaction Steps
To a solution of 3.3 g of 2-(m-iodoanilino)-3-aminomethylpyridine and 30 ml of dry tetrahydrofuran was added 3.2 g of N,N'-carbonyldiimidazole and the mixture was heated under reflux 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 dissolved in acetone. The acetone solution was placed on a column of alumina and eluted with acetone. The eluate was concentrated and left to yield 2.5 g of 1-(m-iodophenyl)-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless needles, melting at 175° - 177° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04009166 |
| Source dataset | uspto-grants-1977_02 |
| ORD ID | ord-b160a19d7d28440c84a267054daef3b3 |
| Source note | uspto-grants-1977_02 |