HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 13435046, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | HCID 13435024 | HCID 13435024 | — |
| Product | HCID 13435046 | HCID 13435046 | — |
Reaction Steps
2-trans-[2-(2-methyl-phenyl)-ethenyl]-3-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine-7-carboxylic acid (1,2 g) was reacted with thionyl chloride (0.6 ml) in dioxane (12 ml) at reflux temperature for 1 hour, then the mixture was evaporated to dryness in vacuo. The residue was reacted with excess methanol at 50° C. for 30 minutes, then the solution was concentrated in vacuo and the residue diluted with ice water. Filtration of the precipitate gave 1.2 g of 2-trans-[2-(2-methyl-phenyl)-ethenyl]-3-propyl-4-oxo-4H-pyrido[1,2-a]pyrimidine7-carboxylic acid, methyl ester, m.p. 190°-193° C. By proceeding analogously the following compounds were prepared:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04310526 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-a284f1ec92794885bf168693d65390f6 |
| Source note | uspto-grants-1982_01 |