Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21452457 | HCID 21452457 | — |
| Reactant | HCID 22020247 | HCID 22020247 | — |
| Reactant | HCID 86734505 | HCID 86734505 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13259312 | HCID 13259312 | 50.8% |
Reaction Steps
To a solution of 2.3 g of 2-(m-fluoroanilino)-3-methylaminomethylpyridine was added 0.96 g of approximately 50% sodium hydride and the mixture was stirred at room temperature for 30 minutes. To this was added 10 g of approximately 30% carbon tetrachloride-phosgene solution, dropwise under ice-cooling, and the resulting mixture was stirred for 1 hour. After an excess of the phosgene was decomposed with 10% acetone-ammonia solution, 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 applied on a column of alumina and then eluted with ether. The eluate was concentrated and left to give 1.3 g of 1-(m-fluorophenyl)-3-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-d]pyrimidine as colorless prisms, melting at 189° - 192° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04009166 |
|---|
| Source dataset | uspto-grants-1977_02 |
|---|
| ORD ID | ord-63932a91f8b444dd8db85069e64563d5 |
|---|
| Source note | uspto-grants-1977_02 |
|---|